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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289404Generated: October 29, 2026

Benzene → HCID 178460459, compound

https://huagongshe.com/reaction/1289404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantHCID 178525421HCID 178525421—
ProductHCID 178460459HCID 17846045933%

Reaction Steps

First, 2.8 g of 13-[trans-4-(2,3-difluorophenyl)cyclohexyl]tridecyl 2,2-bis(6-hydroxyhexyl)acetate, 1 g of triethylamine, and 30 ml of benzene were placed in a 100 ml flask. A small amount of benzene in which 0.9 g of acryloyl chloride was dissolved was added dropwise to the reaction mixture under ice water cooling. The reaction mixture was allowed to warm to room temperature and stirred for 3 hours. The reaction mixture was poured into water, and an organic layer was extracted with ether. The ether layer was washed with diluted hydrochloric acid and water in this order, and then dried over anhydrous sodium sulfate. The solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/toluene=1/20) to obtain 1.12 g of 13-[trans-4-(2,3-difluorophenyl)cyclohexyl]tridecyl 2,2-bis(6-acryloyloxyhexyl)acetate (Y: 33%). The compound thus obtained was liquid at room temperature. The compound had a purity of 99.6% by HPLC and of 1 spot by TLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750213
Source datasetuspto-grants-1998_05
ORD IDord-4d37b84f2d514af59b428c4d93ff8cb3
Source noteuspto-grants-1998_05