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Chemical Structure| 128310-70-3 Chemical Structure| 128310-70-3

Structure of 128310-70-3

Chemical Structure| 128310-70-3

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Product Details of [ 128310-70-3 ]

CAS No. :128310-70-3
Formula : C11H14O3
M.W : 194.23
SMILES Code : O=C(OCC)C1=CC=C([C@H](O)C)C=C1
MDL No. :MFCD28101065

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Application In Synthesis of [ 128310-70-3 ]

* 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 [ 128310-70-3 ]

[ 128310-70-3 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 38430-55-6 ]
  • [ 128310-70-3 ]
YieldReaction ConditionsOperation in experiment
98% With hydrogen;trans-RuH(eta1-BH4)[(S)-xylbinap][(S,S)-dpen]; In isopropyl alcohol; at 25℃; under 6080.41 Torr; for 15h;Conversion of starting material; Chiral hydrogenation of ethyl 4-acetylbenzoate was carried out (see formula (9) below). That is, a reaction was carried out in accordance with the procedures of Example 4 using the (S,SS)-ruthenium hydride complex (1.5 mg; 0.00125 mmol) synthesized in Example 2 and using ethyl 4-acetylbenzoate (961 mg; 5.00 mmol) (Wako.Co.,Ltd.) as the substrate and 2-propanol (5 mL) as the solvent. However, the hydrogen pressure was set to 8 atmosphere, the reaction temperature was set to 25 C., and the reaction time was set to 15 hours. As a result, ethyl (R)-4-(1-hydroxyethyl) benzoate was obtained at a conversion rate of 100%, isolation yield of 98% (951 mg; 4.9 mmol), and enantiomeric excess of 99%. GC (column: Chirasil-DEXCB; column temperature: 150 C.; injection and detection temperature: 250 C.; helium pressure: 49 kPa; tR of ethyl (R)-4-(1-hydroxyethyl) benzoate : 32.2 minutes (99.4%); tR of ethyl (S)-4-(1-hydroxyethyl) benzoate: 35.1 minutes (0.6%)); tR of ethyl 4-acetylbenzoate 35.5 minutes (0%); [alpha]26D: +32.0 (c:0.912; CH3OH); absolute structure: R; literature value: [alpha]21D+32.6 (c:0.873; CH3OH), 98.6% ee (R).
77.2% With dimethylsulfide borane complex; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole; In dichloromethane; toluene; at -20℃; for 1.16667h; To a dry 100 mL three neck flask at room temperature was added dichloromethane (15 mL)A solution of borane dimethyl sulfide (0.7 mL, 7.0 mmol) and (S) -Me-CBS (1 M solution in toluene, 5.7 mL, 6.0 mmol) was directly added and stirred for 60 minutes. At -20 C, a solution of ethyl 4-acetophenone acetate (1.0 g, 5.4 mmol) in methylene chloride (10 mL) was added dropwise over a period of about 10 minutes using a constant-pressure funnel.And an internal temperature of -20 C ± 5 C. The reaction was continued for 1 hour at the same temperature. The reaction was quenched by slow addition of methanol (5 mL), keeping the internal temperature below -20 C ± 5 C. The organic phase was poured off and the organic phase was washed with saturated sodium chloride (30 mL), dried over anhydrous magnesium sulfate, and concentrated in vacuo. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated in vacuo. Washed once. The organic layer was dried over anhydrous sodium sulfate, and the organic layer was concentrated to a solvent-free residue. The resulting product was separated by chromatography (petroleum ether / ethyl acetate = 1/4) to give the final product (R) -1-hydroxyethyl- -benzoic acid ethyl ester (780 mg, 77.2%).
 

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