MeOH tetrahydrofuran → HCID 23113862, 화합물

HRID 1787151노트

반응식

[Br:1][C:2]1[C:12](C)=[CH:11]C(OCC(C)=O)=[C:4]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([CH:21]([CH3:23])[CH3:22])=[CH:17][CH:16]=2)[C:3]=1[CH3:24].[CH3:25]O.[CH2:27]1[CH2:31][O:30][CH2:29][CH2:28]1>>[Br:1][C:2]1[C:3]([CH3:24])=[C:4]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([CH:21]([CH3:23])[CH3:22])=[CH:17][CH:16]=2)[C:31]2[O:30][CH:29]=[C:28]([CH3:25])[C:27]=2[C:12]=1[CH3:11]

참가 물질

반응물 2

HCID 21899815MeOH tetrahydrofuran

HCID 23114331HCID 23114331, 화합물

생성물 1

HCID 23113862HCID 23113862, 화합물수율 84%

실험 절차

Using 1-(4-bromo-1-(2-(4-isopropylbenzyl)-3,5-dimethylphenoxy)acetone obtained in Reference Example 189, the title compound was synthesized in the same manner as in Reference Example 143. Yield 84%. Melting point: 76-77° C. (methanol-THF).

후처리

customobtained in Reference Example 189

출처 및 근거

ORD 기록: ord-36d699658e99427b8f5cb5a7d0356402
출처 데이터셋: uspto-grants-2009_03
DOI: 10.6084/m9.figshare.5104873.v1
특허 번호: US07507841B2

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