Methanesulfonyl chloride → alpha-(1-Benzyl-3-pyrrolidinyl)-alpha,alpha-diphenylacetonitrile
Reaction equation
[C:1]1([CH2:7][N:8]2[CH2:12][CH2:11][CH:10](O)[CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CS(Cl)(=O)=O.[C:19]1([CH:25]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:26]#[N:27])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[Na]>C(N(CC)CC)C>[C:28]1([C:25]([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)([CH:10]2[CH2:11][CH2:12][N:8]([CH2:7][C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[CH2:9]2)[C:26]#[N:27])[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1Participants
5
Procedure
The title compound was prepared from 1-(phenylmethyl)-3-pyrrolidinol, methanesulfonylchloride, triethylamine and sodium diphenylacetonitrile by the procedure of U.S. Pat. No. 3,192,210, b.p. 215-218/0.01 mm.
Sources & evidence
- ORD record
- ord-e9466fe528b24f418812a2d6136c6112
- Source dataset
- uspto-grants-1986_06
- Patent number
- US04594343
Reaction notes
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