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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295348Generated: October 30, 2026

Thionyl Chloride → 2-Phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hexane-1-carbonyl chloride

https://huagongshe.com/reaction/1295348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hexane-1-carboxylic acidHCID 58907323—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
Product2-Phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hexane-1-carbonyl chlorideHCID 58907324101.4%

Reaction Steps

To a stirring solution of racemic 2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hexane-1-carboxylic acid (1.5 g, 4.2 mmol) (Intermediate 2) and one drop DMF in 10 mL of toluene at 0° C. was added thionyl chloride (8.6 mL, 11.8 mmol). The reaction was allowed to warm to room temperature and then heated to 73° C. for 2.5 hours. The solvent and excess thionyl chloride were evaporated at reduced pressure to leave 2-phenyl-3-(toluene-4-sulfonyl)-3-aza-bicyclo[3.1.0]hexane-1-carbonyl chloride (1.6 g, 100% crude yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241798B2
Source datasetuspto-grants-2007_07
ORD IDord-fc80d2c898b8440296948e66f23d4bb4
Source noteuspto-grants-2007_07