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Tetrahydrofuran → (3-Tert-butyl-2-methoxy-5-ethylphenyl)dimethyl(tetramethylcyclopentadienyl)silane

HRID 634880
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반응식

HRID 634880 반응식
[C:1]([C:5]1[C:6]([O:16][CH3:17])=[C:7]([Si:12](Cl)([CH3:14])[CH3:13])[CH:8]=[C:9]([CH3:11])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:18][C:19]1[CH:23]([Li])[C:22]([CH3:25])=[C:21]([CH3:26])[C:20]=1[CH3:27].O1CCC[CH2:29]1>>[C:1]([C:5]1[C:6]([O:16][CH3:17])=[C:7]([Si:12]([CH3:14])([CH3:13])[C:22]2([CH3:25])[CH:23]=[C:19]([CH3:18])[C:20]([CH3:27])=[C:21]2[CH3:26])[CH:8]=[C:9]([CH2:11][CH3:29])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 8028TetrahydrofuranHCID 11032947(2-Methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane2회HCID 178506838Lithium tetramethylcyclopentadienide

생성물 1

HCID 131722375(3-Tert-butyl-2-methoxy-5-ethylphenyl)dimethyl(tetramethylcyclopentadienyl)silane

실험 절차

To a solution of (3-tert-butyl-2-methoxy-5-methylphenyl)chlorodimethylsilane (5.24 g) synthesized in the above (3) and tetrahydrofuran (50 ml), tetramethylcyclopentadienyl lithium (2.73 g) was added at −35° C. and the mixture was heated to room temperature over 2 hours, followed by stirring at room temperature for 10 hours.

후처리

  1. additionwas added at −35° C.

출처 및 근거

ORD 기록
ord-440b0fd3f3e74778924a7df8cc9b24b5
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06184319B2

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