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Ethanol → HCID 14597164, 화합물

HRID 2051450
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HRID 2051450 반응식
[C:1]([C:4]1[CH:19]=[CH:18][C:7]([C:8]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:9])=[CH:6][CH:5]=1)(=[O:3])[CH3:2].C(O)C.[BH4-].[Na+]>C(Cl)(Cl)Cl>[OH:3][CH:1]([C:4]1[CH:19]=[CH:18][C:7]([C:8]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:9])=[CH:6][CH:5]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 590101Benzyl 4-acetylbenzoateHCID 4311764Sodium borohydride

생성물 1

HCID 14597164HCID 14597164, 화합물수율 95%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

60.98 g (0.24 mol) of benzyl 4-acetylbenzoate (II-19), 100 ml of ethanol and 300 ml of chloroform were supplied into a four-necked flask equipped with a stirrer and a thermometer. Then 4.6 g (0.12 mol) of sodium borohydride was added at 15°-25° C. over a period of 10 minutes. The mixture was kept at the same temperature for 2 hours and the resulting reaction mixture was poured into ice-water and extracted twice with 200 ml of ethyl acetate. The organic layer was washed with water and concentrated under reduced pressure to obtain 58.37 g (95% yield) of benzyl 4-(1-hydroxyethyl)phenylcarboxylate (III-19). nD25 =1.5682.

후처리

  1. customequipped with a stirrer
  2. customthe resulting reaction mixture
  3. extractionextracted twice with 200 ml of ethyl acetate
  4. washThe organic layer was washed with water
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-f4ed24f95c4f4927af053c25c545060f
출처 데이터셋
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05019298

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