(2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride

Base Information

Chemical Name:(2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride
CAS No.:1192649-53-8
Molecular Formula:C₂₁H₂₂FNO₂*ClH
Molecular Weight:375.871
Hs Code.:

Synonyms:(2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride

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Chemical Property of (2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride

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Technology Process of (2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride

There total 1 articles about (2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 76.0%

: 1192649-50-5
methyl (2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylate

: 1192649-53-8
(2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride

Guidance literature:: methyl (2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylate; With ethanol; sodium hydroxide; at 20 ℃; for 24h;

With hydrogenchloride; water; In ethanol; pH=5 - 6;
DOI:10.1016/j.bmc.2009.08.010

Reference yield: 81.0%

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: 1192649-53-8
(2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride

: 1192649-57-2
(2S,4R)-2-diazoacetyl-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine

Guidance literature:: (2S,4R)-1-(4,4-diphenyl-3-butenyl)-4-fluoropyrrolidine-2-carboxylic acid hydrochloride; With sodium hydroxide; In ethanol;

With triethylamine; isobutyl chloroformate; In dichloromethane; at -20 ℃;

diazomethane; In dichloromethane; at 0 ℃;
DOI:10.1016/j.bmc.2009.08.010