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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289380Generated: November 4, 2026

Water → 2,3-Difluoro-4'-[12,12-bis(acryloyloxymethyl)dodecyl]oxybiphenyl

https://huagongshe.com/reaction/1289380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant2,3-Difluoro-4'-[12,12-bis(hydroxymethyl)dodecyl]oxybiphenylHCID 18920846—
Product2,3-Difluoro-4'-[12,12-bis(acryloyloxymethyl)dodecyl]oxybiphenylHCID 1892086857%

Reaction Steps

First, 2.4 g of 2,3-difluoro-4'-[12,12-bis(hydroxymethyl)dodecyl]oxybiphenyl, 1.3 g of triethylamine, and 100 ml of tetrahydrofuran were placed in a 200 ml flask. Then, 15 ml of tetrahydrofuran solution in which 1.1 g of acryloyl chloride was dissolved was added dropwise to the reaction mixture under ice water cooling, and 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: toluene/ethyl acetate=20/1) and recrystallized from hexane to obtain 1.7 g of 2,3-difluoro-4'-[12,12-bis(acryloyloxymethyl)dodecyl]oxybiphenyl (Y: 57%). The compound thus obtained had a purity of 99.6% by GC, 100% by HPLC, and 1 spot by TLC. The compound thus obtained had an m.p. of 33.4° C. to 34.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750213
Source datasetuspto-grants-1998_05
ORD IDord-555dcde752ec4a2593cb9152ed174dc0
Source noteuspto-grants-1998_05