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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289391Generated: November 1, 2026

Benzene → 11-[2,3Difluorobiphenyl-4'-yl]oxyundecyl 2,2-bis(6-acryloyloxyhexyl)acetate

https://huagongshe.com/reaction/1289391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant11-[2,3-Difluorobiphenyl-4'-yl]oxyundecyl 2,2-bis(6-hydroxyhexyl)acetateHCID 18920835—
Product11-[2,3Difluorobiphenyl-4'-yl]oxyundecyl 2,2-bis(6-acryloyloxyhexyl)acetateHCID 1892084932%

Reaction Steps

First, 3.66 g of 11-[2,3-difluorobiphenyl-4'-yl]oxyundecyl 2,2-bis(6-hydroxyhexyl)acetate, 1.3 g of triethylamine, and 30 ml of benzene were placed in a 100 ml flask. Then, a small amount of benzene in which 1.2 g of acryloyl chloride was dissolved was added dropwise to the reaction mixture under ice water cooling. The resultant 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. Thereafter, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/toluene=1/20) to obtain 1.36 g of 11-[2,3difluorobiphenyl-4'-yl]oxyundecyl 2,2-bis(6-acryloyloxyhexyl)acetate (Y: 32%). The compound thus obtained was liquid at room temperature. The compound thus obtained had a purity of 99% 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-01897ce5ef054f13a88ecc58e7b9cf9e
Source noteuspto-grants-1998_05