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Acetic Anhydride → Acetic acid 7-(tert-butyl-dimethyl-silanyloxy)-hept-2-ynyl ester

HRID 406802
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인쇄 미리보기

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HRID 406802 반응식
[C:1]([Si:5]([CH3:16])([CH3:15])[O:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]#[C:12][CH2:13][OH:14])([CH3:4])([CH3:3])[CH3:2].[C:17](OC(=O)C)(=[O:19])[CH3:18]>N1C=CC=CC=1>[C:1]([Si:5]([CH3:16])([CH3:15])[O:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]#[C:12][CH2:13][O:14][C:17](=[O:19])[CH3:18])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 111725557-(tert-Butyl-dimethyl-silanyloxy)-hept-2-yn-1-ol

생성물 1

HCID 86593935Acetic acid 7-(tert-butyl-dimethyl-silanyloxy)-hept-2-ynyl ester

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 7-(tert-Butyl-dimethyl-silanyloxy)-hept-2-yn-1-ol 27 (4.507 g, 21 mmol) in pyridine (20 mL) was treated with acetic anhydride (3.0 mL, 31.8 mmol). After 18 h, the solvent was evaporated and the residue co-evaporated with toluene. The residue was used directly in the next step.

후처리

  1. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-42a6b61595b7438db7b578a60adafa1c
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08754122B2

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