반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:20]Br.[Cl:22][C:23]1[CH:28]=[CH:27][C:26]([CH2:29][CH2:30][CH2:31]O)=[CH:25][CH:24]=1.N1C=CC=CC=1>C1(C)C=CC=CC=1.C(OCC)C.CCCCCC>[Cl:22][C:23]1[CH:28]=[CH:27][C:26]([CH2:29][CH2:30][CH2:31][Br:20])=[CH:25][CH:24]=1참가 물질
8
실험 절차
To a stirred solution of 4.15 g (15.8 mmol) of triphenylphosphine in 100 ml of toluene at 0° C., 1.51 ml (15.8 mmol) of bromine was added dropwise. This mixture was stirred for 3 hours then a solution of 3.90 g (22.9 mmol) of Part (a) alcohol and 1.63 ml (15.8 mmol) of pyridine in 20 ml of toluene was added. A solution of 25 ml hexane and 25 ml diethyl ether was added, and a brown mass was formed. The liquid was decanted and concentrated in vacuo. The residue was triturated with hexane:ethyl acetate and triphenylphosphine oxide was precipitated. The solid was filtered and the filtrate was concentrated in vacuo to give a yellow oil. The oil was purified by flash chromatography to obtain 1.80 g (7.72 mmol, 49%) of the desired product.
후처리
- customa brown mass was formed
- customThe liquid was decanted
- concentrationconcentrated in vacuo
- customThe residue was triturated with hexane
- customethyl acetate and triphenylphosphine oxide was precipitated
- filtrationThe solid was filtered
- concentrationthe filtrate was concentrated in vacuo
- customto give a yellow oil
- customThe oil was purified by flash chromatography
출처 및 근거
- ORD 기록
- ord-6614be92edb84379ae0cd133291ddd7d
- 출처 데이터셋
- uspto-grants-1992_10
- 특허 번호
- US05153327
연결된 노트
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