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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241830Generated: November 3, 2026

Water → HCID 68546191, compound

https://huagongshe.com/reaction/2241830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Chloro-4-fluorobenzonitrileHCID 109000—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductHCID 68546191HCID 68546191—

Reaction Conditions

Temperature5 °C

Reaction Steps

A 1.0 M solution of potassium t-butoxide in t-butanol (3.2 mL) was added to a 16 mL vial fitted with a septa cap containing 3 mL of dry THF and 300 mg (3 mmoles) of cis-1,2-dihydroxy cylcopentanol at 5° C. The mixture was stirred for 0.5 h at 5° C., after which time 3 mL of a 1.0 M THF solution of 4-fluoro-2-chloro-benzonitrile was added. The reaction was stirred at 5° C. for 3 h and then allowed to warm to room temperature and stirred overnight at room temperature. The reaction mixture was cooled to 0° C., poured into a seperatory funnel containing 15 mL of water, and extracted with 20 mL of methyl tert-butyl ether. The organic phase was washed with water, brine, dried (MgSO4), concentrated in vacuo, and the residue purified by reverse phase HPLC (Shimadzu) to give 185 mg 2-Chloro-4-(cis-2-hydroxy-cyclopentyloxy)-benzonitrile. GC/MS: 237 (M/Z for C13H14ClNO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07670613B2
Source datasetuspto-grants-2010_03
ORD IDord-50e515f642594d17866906c48abed5ef
Source noteuspto-grants-2010_03