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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154399Generated: October 31, 2026

Pyridine → HCID 86739798, compound

https://huagongshe.com/reaction/1154399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrileHCID 9837437—
ReactantHCID 86739799HCID 86739799—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86739798HCID 8673979820.1%

Reaction Steps

0.9 ml of pyridine and 2 g of dicyclohexylcarbodiimide were added to a solution of 2.6 g of the product of Step A in 40 ml of methylene chloride and the mixture was stirred for 10 minutes. 2 g of (S)α-cyano-3-phenoxy-benzyl alcohol were added to the mixture which was stirred for 10 minutes after which 25 mg of 4-dimethylamino-pyridine were added thereto. The mixture was stirred for 90 minutes and was filtered and the filtrate was evaporated to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with a 95-5 cyclohexane-ethyl acetate mixture to obtain 0.743 g of (S)α-cyano-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3(E)-[2-propoxycarbonyl-ethenyl]-cyclopropane-1-carboxylate and 3.64 g of a mixture. The latter was dissolved in 4 volumes of hot isopropyl ether and the mixture was stirred at 20° C. and was then vacuum filtered to obtain another 2.32 g of the desired ester melting at 68° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489093
Source datasetuspto-grants-1984_12
ORD IDord-ade7886a92684b9790db961b753e81d6
Source noteuspto-grants-1984_12