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Triethylamine → 5-(2-Methylbenzoyloxy)indan

HRID 258039
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반응식

HRID 258039 반응식
[OH:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH2:7][CH2:6][CH2:5]2.C(N(CC)CC)C.[CH3:18][C:19]1[CH:27]=[CH:26][CH:25]=[CH:24][C:20]=1[C:21](Cl)=[O:22]>ClCCl>[CH3:18][C:19]1[CH:27]=[CH:26][CH:25]=[CH:24][C:20]=1[C:21]([O:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH2:7][CH2:6][CH2:5]2)=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 151185-IndanolHCID 702762-Methylbenzoyl chloride

생성물 1

HCID 99923955-(2-Methylbenzoyloxy)indan

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To an ice-cooled mixture of 5-hydroxyindan (13.4 g), triethylamine (14.0 ml) and dichloromethane (150 ml) was added 2-methylbenzoyl chloride (15.4 ml) dropwise with constant stirring. The mixture was further stirred under ice-cooling for one hour, after which it was washed with water and dried (MgSO4). The solvent was then distilled off to give 5-(2-methylbenzoyloxy)indan as oil in quantitative yield.

후처리

  1. temperaturecooling for one hour
  2. washafter which it was washed with water
  3. dry with materialdried (MgSO4)
  4. distillationThe solvent was then distilled off

출처 및 근거

ORD 기록
ord-16f1cb2dd9f342298b30a69d765b3c9d
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05264454

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