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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025326Generated: October 31, 2026

Propionitrile → HCID 66771118, compound

https://huagongshe.com/reaction/1025326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionitrileHCID 7854—
ReactantTriethylamineHCID 8471—
Reactanto-ChlorothiophenolHCID 80599—
ReactantHCID 86646817HCID 86646817—
SolventSodium CarbonateHCID 10340—
ProductHCID 66771118HCID 66771118—

Reaction Conditions

Temperature100 °C

Reaction Steps

Under an atmosphere of argon, (2S,4S)-1-tert-butyl 2-methyl 4-(3-nitrophenylsulfonyloxy)pyrrolidine-1,2-dicarboxylate (8.5 g, 19.7 mmol, Eq: 1.00) was combined with propionitrile (82.0 ml) to give a light brown solution. Then 2-chlorobenzenethiol (4.28 g, 3.38 ml, 29.6 mmol, Eq: 1.50) and triethylamine (4.00 g, 5.5 ml, 39.5 mmol, Eq: 2.00) were added dropwise. The reaction was stirred overnight at reflux (100° C.). The reaction was cooled to room temperature, and poured in 50 ml Na2CO3 solution (10%), and extracted with 2×100 ml ethyl acetate. The organic layers were washed with 50 ml HCl 0.1M and 50 ml satd. NaCl solution. The organic layer was stirred over Na2SO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography (70 g column, from 100% to 80% heptane in ethyl acetate). The title compound was obtained as a yellow oil (5.7 g, 77.6%, MS (m/e)=372.1 [M+H+]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729061B2
Source datasetuspto-grants-2014_05
ORD IDord-6f2bfb9600a74525b221206813b0f448
Source noteuspto-grants-2014_05