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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726510Generated: October 30, 2026

Tetrahydrofuran → HCID 178460515, compound

https://huagongshe.com/reaction/726510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantHCID 178521549HCID 178521549—
SolventWaterHCID 962—
ProductHCID 178460515HCID 17846051552.6%

Reaction Steps

First, 4.24 g of trans-4-(2,3-difluorophenyl)cyclohexanol, 2 g of triethylamine, and 60 ml of tetrahydrofuran were placed in a 100 ml flask. Then, 2.3 g of acryloyl chloride was added dropwise to the mixture under ice water cooling. The mixture was stirred at the same temperature for 3 hours. Water was added to the reaction mixture, and an organic layer was extracted with ether. The ether layer was washed with water and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: benzene/hexane=1/1) and recrystallized from hexane to obtain 2.8 g of trans-4-(2,3-difluorophenyl)cyclohexyl acrylate (Y: 52.6%). The compound thus obtained had a purity of 99.9% by GC and 99.5% by HPLC. Furthermore, the compound had an m.p. of 72.9° C. to 73.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05709911
Source datasetuspto-grants-1998_01
ORD IDord-5987429c551945a099f57d037f81d7dd
Source noteuspto-grants-1998_01