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2-Mercaptoethanol → HCID 54425911, 화합물

HRID 1109411
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HRID 1109411 반응식
[C:1]1([CH2:11][C:12](=[CH2:18])[C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.CC(C)([O-])C.[K+].[SH:25][CH2:26][CH2:27][OH:28]>C(OCC)C>[OH:28][CH2:27][CH2:26][S:25][CH2:18][CH:12]([CH2:11][C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1)[C:13]([O:15][CH2:16][CH3:17])=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 15672-Mercaptoethanol2회HCID 11776435HCID 11776435, 화합물HCID 23665647Potassium tert-butoxide

생성물 1

HCID 54425911HCID 54425911, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

2.04 g of ethyl 2-(1-naphthyl)methyl-2-propenoate was dissolved in 714 μl of 2-mercaptoethanol, and 102 mg of potassium tert-butoxide was added thereto at room temperature under stirring. The mixture was stirred at room temperature for 15 minutes. 500 μl of 2-mercaptoethanol was added thereto and the mixture was stirred for 15 minutes. Then, the reaction solution was diluted with 150 ml of diethyl ether. The diethyl ether layer was washed with water and with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain 2.81 g of ethyl (2RS)-3-(2-hydroxyethyl)thio-2-(1-naphthylmethyl)propionate as colorless oily substance.

후처리

  1. stirringThe mixture was stirred at room temperature for 15 minutes
  2. stirringthe mixture was stirred for 15 minutes
  3. washThe diethyl ether layer was washed with water and with a saturated sodium chloride aqueous solution
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationThe solvent was distilled off

출처 및 근거

ORD 기록
ord-8d2ddaa0ef8d4cf0940aa17a423b453f
출처 데이터셋
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05319082

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