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Pyridine → 2,2-Dimethylpropyl 2-methyl-4-bromobenzoate

HRID 51735
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인쇄 미리보기

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HRID 51735 반응식
[CH3:1][C:2]1[CH:10]=[C:9]([Br:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12][C:13]([CH3:17])([CH3:16])[CH2:14]O.N1C=CC=CC=1>O=S(Cl)Cl>[CH3:1][C:2]1[CH:10]=[C:9]([Br:11])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH2:12][C:13]([CH3:17])([CH3:16])[CH3:14])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 6404Neopentyl alcoholHCID 995704-Bromo-2-methylbenzoic acid

생성물 1

HCID 225689392,2-Dimethylpropyl 2-methyl-4-bromobenzoate수율 68%

시약·촉매·용매 1

HCID 24386Thionyl Chloride용매

실험 절차

Using General Esterification Method C; 2-methyl-4-bromo-benzoic acid (1.82 g, 8.47 mmols) was refluxed for 3 h with 10 mL SOCl2. The resulting solution was concentrated under reduced pressure and the crude acyl chloride combined with 2,2-dimethylpropanol (0.75 g, 8.47 mmols) and pyridine (1.4 mL, 16.9 mmols) to give the title compound (1.64 g, 68%) after work-up and column chromatography (2-5% EtOAc-hexanes) as a colorless oil.

후처리

  1. concentrationThe resulting solution was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-f45be08afa6b41319c22b38d8a4a62e9
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06713647B2

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