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N,N-Dimethylaniline → 2,6,10,10-Tetramethyl-1-oxa-spiro[4.5]dec-6-yl butyrate

HRID 1856306
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반응식

HRID 1856306 반응식
[CH3:1][CH:2]1[CH2:6][CH2:5][C:4]2([C:11]([CH3:13])([CH3:12])[CH2:10][CH2:9][CH2:8][C:7]2([CH3:15])[OH:14])[O:3]1.CN(C)C1C=CC=CC=1.[C:25](Cl)(=[O:29])[CH2:26][CH2:27][CH3:28]>>[C:25]([O:14][C:7]1([CH3:15])[CH2:8][CH2:9][CH2:10][C:11]([CH3:13])([CH3:12])[C:4]21[O:3][CH:2]([CH3:1])[CH2:6][CH2:5]2)(=[O:29])[CH2:26][CH2:27][CH3:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 949N,N-DimethylanilineHCID 8855Butyryl chlorideHCID 654286-Hydroxydihydrotheaspirane

생성물 1

HCID 233465732,6,10,10-Tetramethyl-1-oxa-spiro[4.5]dec-6-yl butyrate수율 57%

실험 절차

2.12 g (0.01 M) of 2,6,10,10-tetramethyl-1-oxa-spiro[4.5]decan-6-ol--isomer A; see Example 1--were treated with a mixture of 12.1 g (0.1 M) of N,N-dimethylaniline and 5.3 g (0.05 M) of butyryl chloride as indicated in Example 3--except heating at 100° for 3 hours--to give 1.6 g (57%) of the desired ester, b.p. 120°/0.5 Torr.

후처리

  1. temperatureexcept heating at 100° for 3 hours
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출처 및 근거

ORD 기록
ord-16c839c9d6524bd29910546f8b79f372
출처 데이터셋
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04218488

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