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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569550Generated: October 30, 2026

2-(4-Fluoro-3-phenoxyphenyl)-2-hydroxyacetonitrile → (S)alpha-cyano-3-phenoxy-4-fluoro-benzyl(1R,cis,Z)2,2-dimethyl-3-[3-oxo-3-tert.-butoxy-1-propenyl]-cyclopropanecarboxylate

https://huagongshe.com/reaction/569550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Fluoro-3-phenoxyphenyl)-2-hydroxyacetonitrileHCID 10377109—
Reactant(1R,cis,Z) 2,2-dimethyl-3-[3-oxo-3-tert.-butoxy-1-propenyl]-cyclopropane-carboxylic acidHCID 13269380—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(S)alpha-cyano-3-phenoxy-4-fluoro-benzyl(1R,cis,Z)2,2-dimethyl-3-[3-oxo-3-tert.-butoxy-1-propenyl]-cyclopropanecarboxylateHCID 1318840593.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 30 g of (RS)α-cyano-3-phenoxy-4-fluoro-benzyl alcohol, 300 mg of 4-dimethylamino-pyridine and 50 ml of methylene chloride was added all at once at -5° C. to a solution of 30 g of (1R,cis,Z)2,2-dimethyl-3-[3-oxo-3-tert.-butoxy-1-propenyl]-cyclopropane-carboxylic acid in 100 ml of methylene chloride and the mixture was stirred at 0° C. for 30 minutes and at 20° C. for 3 hours. The mixture was filtered and the filtrate was evaporated to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with an 8-2 n-hexane-ethyl acetate mixture to obtain 53.9 g of (S)α-cyano-3-phenoxy-4-fluoro-benzyl(1R,cis,Z)2,2-dimethyl-3-[3-oxo-3-tert.-butoxy-1-propenyl]-cyclopropanecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732903
Source datasetuspto-grants-1988_03
ORD IDord-72b63a00e26a43d2afc0c273e28efe70
Source noteuspto-grants-1988_03