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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154398Generated: November 4, 2026

Pyridine → HCID 86739796, compound

https://huagongshe.com/reaction/1154398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrileHCID 9837437—
ReactantHCID 86739797HCID 86739797—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86739796HCID 8673979687.5%

Reaction Steps

0.9 ml of pyridine and 2.1 g of dicyclohexylcarbodiimide were added to a solution of 2.9 g of the product of Step B in 40 ml of methylene chloride and the mixture was stirred for 15 minutes. A solution of 2.5 g of (S)α-cyano-3-phenoxy-benzyl alcohol in 15 ml of methylene chloride and then 25 mg of 4-dimethylamino-pyridine were added to the reaction mixture which was stirred for 2 hours and filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with a 9-1 cyclohexane-ethyl acetate mixture yielded 4.26 g of (S)α-cyano-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3(Z)-[2-bromo-2-propoxycarbonyl-ethenyl]-cyclopropane-1-carboxylate melting at 64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489093
Source datasetuspto-grants-1984_12
ORD IDord-e3989a5f1f9b4a9889e15b00ebec372f
Source noteuspto-grants-1984_12