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Chemical Structure| 1212182-03-0 Chemical Structure| 1212182-03-0

Structure of 1212182-03-0

Chemical Structure| 1212182-03-0

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Product Details of [ 1212182-03-0 ]

CAS No. :1212182-03-0
Formula : C11H21NO3
M.W : 215.29
SMILES Code : OCC[C@@H]1CN(C(OC(C)(C)C)=O)CC1
MDL No. :MFCD09608025

Safety of [ 1212182-03-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H317
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 1212182-03-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1212182-03-0 ]

[ 1212182-03-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 204688-60-8 ]
  • [ 1212182-03-0 ]
YieldReaction ConditionsOperation in experiment
100% Borane-THF complex (3.90 kg or L of 1 M in THF, mol) was added slowly to a stirred solution of (R)-2-(1-(terf-butoxycarbonyl)pyrrolidine-3-yl)acetic acid (683 g, 3.03 mol) in THF (2.5 kg), kept under nitrogen gas, and using a water bath to keep the temperature between 23 and 28 C. The addition took 1.75 h. Stirring at 25 C was continued for 1 h, after which time GC analysis indicated complete reaction. The reaction mixture was cooled to <10 C and maintained below 25 C as 10% aqueous sodium hydroxide (1.22 kg) was slowly added. The addition took 40 min. The mixture was stirred 1 h at 25 C, and then combined with 1 :1 (v/v) heptane/ethyl acetate (7 L). The mixture was stirred for 15 min and allowed to separate into phases (1 h). The organic phase was withdrawn, and the aqueous phase was combined with a second 7 L portion of 1 :1 heptane/ethyl acetate. This was stirred for 15 min and allowed to separate into phases (20 min). The organic phase was again withdrawn, and the combined organic phases were washed with saturate aqueous sodium chloride (4.16 kg), using 15 min of mixing and 1 h of settling time. The organic phase was combined with silica gel (140 g) and stirred 1 h. The anhydrous sodium sulfate (700 g) was added, and the mixture was stirred for 1.5 h. The mixture was filtered, and the filter cake was washed with 1 :1 heptane/ethyl acetate (2 L). The filtrate was concentrated under vacuum at <40 C for 6 h. The resulting oil weighed 670 g (103% yield) and contains traces of heptane, but is otherwise identical to previously prepared samples of 6, by NMR analysis.
91.3% Example 6. Synthesis of tert-butyl (R)-3-(2-hydroxyethyl)pyrrolidine-1-carboxylate (6); Procedure A; A solution of (R)-2-(1-(feAt-butoxycarbonyl)pyrroliotadiotane-3-yl)acetiotac acid (49 0 g, 214 mmol) in tetrahydrofuran (THF) (200 mL) was cooled to -10 0C 250 mL (250 mmol) of a 1 M borane in THF solution was added slowly to the flask while maintaining the temperature lower than 0 C The solution was warmed to ambient temperature and stirred for 1 h The solution was sampled hourly and analyzed by HPLC to establish completion of the reaction Upon completion of the reaction, the solution was cooled to 0 0C, and a 10% sodium hydroxide solution (80 mL) was added drop-wise over a 30 minute period to control gas evolution The solution was extracted with 500 mL of a 1 1 hexanes/ethyl acetate solution The organic layer was washed with saturated sodium chloride solution and dried with 10 g of silica gel The silica gel was removed by filtration and washed with 100 mL of 1 1 hexanes/ethyl acetate The organic layers were combined and concentrated under vacuum to give 6 (42 g, 91 3 %) as a light-orange oil that solidified upon sitting 1H NMR (CDCI3, 400 MHz) delta 3 67 (m, 2H), 3 38-3 62 (m, 2H), 3 25 (m, 1 H), 2 90 (m, 1 H), 2 25 (m, 1 H), 1 98-2 05 (m, 1 H) 1 61-1 69 (m, 2H), 1 48-1 59 (m, 2H), 1 46 (s, 9H)
91.3% Example 6. Synthesis of tert-butyl (R)-3-(2-hydroxyethyl)pyrrolidine-1- carboxylate (6)Procedure A: A solution of (R)-2-(1-(terf-butoxycarbonyl)pyrrolidine-3- yl)acetic acid (49.0 g, 214 mmol) in tetrahydrofuran (THF) (200 mL) was cooled to - 10 0C. 250 mL (250 mmol) of a 1 M borane in THF solution was added slowly to the flask while maintaining the temperature lower than 0 0C. The solution was warmed to ambient temperature and stirred for 1 h. The solution was sampled hourly and analyzed by HPLC to establish completion of the reaction. Upon completion of the reaction, the solution was cooled to 0 0C, and a 10% sodium hydroxide solution (80 mL) was added drop-wise over a 30 minute period to control gas evolution. The solution was extracted with 500 mL of a 1 :1 hexanes/ethyl acetate solution. The organic layer was washed with saturated sodium chloride solution and dried with 10 g of silica gel. The silica gel was removed by filtration and washed with 100 mL of 1 :1 hexanes/ethyl acetate. The organic layers were combined and concentrated under vacuum to give 6 (42 g, 91.3 %) as a light-orange oil that solidified upon sitting. 1H NMR (CDCI3, 400 MHz) delta 3.67 (m, 2H), 3.38-3.62 (m, 2H), 3.25 (m, 1 H), 2.90 (m, 1 H), 2.25 (m, 1 H), 1.98-2.05 (m, 1 H), 1.61-1.69 (m, 2H), 1.48-1.59 (m, 2H), 1.46 (s, 9H).
 

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