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Chemical Structure| 183793-49-9 Chemical Structure| 183793-49-9

Structure of 183793-49-9

Chemical Structure| 183793-49-9

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Product Details of [ 183793-49-9 ]

CAS No. :183793-49-9
Formula : C9H19NO4
M.W : 205.25
SMILES Code : O=C(OC(C)(C)C)N[C@@H](COC)CO
MDL No. :MFCD20261174
InChI Key :CMWJWKLWQJMPMM-SSDOTTSWSA-N
Pubchem ID :15287812

Safety of [ 183793-49-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362

Application In Synthesis of [ 183793-49-9 ]

* 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 [ 183793-49-9 ]

[ 183793-49-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 51293-47-1 ]
  • [ 543-27-1 ]
  • [ 183793-49-9 ]
YieldReaction ConditionsOperation in experiment
58% B. (R)-tert-Butyl 1-hydroxy-3-methoxypropan-2-ylcarbamate To a mixture of <strong>[51293-47-1](S)-2-(tert-butoxycarbonylamino)-3-methoxypropanoic acid</strong> (10.9 g) and N-methylmorpholine (5.6 g, 55 mmol) in THF (50 mL) was added 2-methylpropylchloroformate (7.48 g, 55 mmol) in THF at -15° C. The reaction mixture was stirred -15° C. for 15 min, after which NaBH4 (6.0 g, 159 mmol) in water (10 mL) was added. The reaction mixture was stirred for 30 min, then diluted with EtOAc, and neutralized with dilute HCl. The organic layer was dried over Na2SO4 and concentrated. The residue was purified by column chromatography on silica gel eluting with EtOAc and petroleum ether (EtOAc/PE=1.5/1) to give the title compound (6.0 g, 58percent). 1H NMR (400 MHz, CDCl3) delta ppm 5.23 (s, 1H), 3.80 (d, J=8.0 Hz, 2H), 3.72-3.68 (m, 1H), 3.60-3.52 (m, 2H), 3.38 (s, 3H), 2.85 (s, 1H), 1.47 (s, 9H).
  • 2
  • [ 51293-47-1 ]
  • [ 183793-49-9 ]
YieldReaction ConditionsOperation in experiment
54.5% isoButyl chloroformate (0.599 mL, 4.56 mmol) was added dropwise to (S)-2-((tert- butoxycarbonyl)amino)-3-methoxypropanoic acid (1 g, 4.56 mmol) and Nmethylmorpholine (0.50 1 mL, 4.56 mmol) in THF (6 mL) and cooled to 0 °C over a period of 15 minutes under nitrogen. The resulting suspension was stirred at 0 °C for a further 15minutes. Sodium borohydride (0.500 g, 13.23 mmol) dissolved in water (1.200 mL) was added slowly to the reaction at 0 °C. The reaction was stirred for 30 minutes before being diluted with EtOAc (50 mL) and neutralised with aqueous HC1 (2M). Water was added (50 mL) and the organic layer was separated, washed with brine (5OmL) and dried over Mg504. The evaporation of the solvent gave a crude product which was purified by flashsilica chromatography, elution gradient 0 to 50percent EtOAc in heptane. Pure fractions were evaporated to dryness to afford (R)-tert-butyl (1 -hydroxy-3-methoxypropan-2- yl)carbamate (0.5 10 g, 54.5 percent) as a colourless oil. ?H NMR (500 MHz, CDC13, 27°C) 1.45 (9H, s), 3.36 (3H, s), 3.5-3.62 (2H, m), 3.64- 3.73 (1H, m), 3.74 - 3.84 (2H, m), 5.16 (1H, s). mlz: ES+ [M+Na]+ 228.
54.5% iso-Butyl chloro formate (0.599 mL, 4.56 mmol) was added dropwise to (S)-2-((tert- butoxycarbonyl)amino)-3-methoxypropanoic acid (1 g, 4.56 mmol) and N- methylmorpholine (0.501 mL, 4.56 mmol) in THF (6 mL) and cooled to 0 °C over a period of 15 minutes under nitrogen. The resulting suspension was stirred at 0 °C for a further 15 minutes. Sodium borohydride (0.500 g, 13.23 mmol) dissolved in water (1.2 mL) was added slowly to the reaction at 0 °C. The reaction was stirred for 30 minutes before being diluted with EtOAc (50 mL) and neutralised with aqueous HC1 (2M). Water was added (50 mL) and the organic layer was separated, washed with brine (50mL) and dried over MgS04. The evaporation of the solvent gave a crude product which was purified by flash silica chromatography, elution gradient 0 to 50percent EtOAc in heptane. Pure fractions were evaporated to dryness to afford (R)-tert-butyl (l-hydroxy-3-methoxypropan-2- yl)carbamate (Intermediate 59; 0.510 g, 54.5percent) as a colourless oil. H NMR (500 MHz, CDCls, 27 °C) 1.45 (9H, s), 3.36 (3H, s), 3.5 - 3.62 (2H, m), 3.64 - 3.73 (1H, m), 3.74 - 3.84 (2H, m), 5.16 (1H, s). m/z: ES+ [M+Na]+ 228
 

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