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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289396Generated: October 30, 2026

Acrylic Acid → 16-[2,3-Difluorobiphenyl-4'-yl]oxyhexadecyl 2,2-bis(6-acryloyloxyhexyl)acetate

https://huagongshe.com/reaction/1289396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
ReactantTriphenylphosphineHCID 11776—
Reactant16-[2,3-Difluorobiphenyl-4'-yl]oxyhexadecyl 2,2-bis(6-hydroxyhexyl)acetateHCID 18920873—
ReactantN-ethoxycarbonyliminocarbamateHCID 86599450—
SolventTetrahydrofuranHCID 8028—
Product16-[2,3-Difluorobiphenyl-4'-yl]oxyhexadecyl 2,2-bis(6-acryloyloxyhexyl)acetateHCID 1892084868.6%

Reaction Steps

First, 3.4 g of 16-[2,3-difluorobiphenyl-4'-yl]oxyhexadecyl 2,2-bis(6-hydroxyhexyl)acetate, 3 g of triphenylphosphine, 0.9 g of acrylic acid, and 30 ml of tetrahydrofuran were placed in a 100 ml flask. Then, 10 ml of a solution in which 2 g of ethyl azodicarboxylate was dissolved in tetrahydrofuran was added dropwise to the mixture under ice water cooling. The resultant mixture was allowed to warm to room temperature and stirred for 3 hours. The reaction mixture was concentrated. Thereafter, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/toluene=1/20) and recrystallized from hexane to obtain 2.7 g of 16-[2,3-difluorobiphenyl-4'-yl]oxyhexadecyl 2,2-bis(6-acryloyloxyhexyl)acetate (Y: 59.7%). The compound thus obtained had a purity of 99% by HPLC and of 1 spot by TLC. The compound had an m.p. of 33.8° C. to 35.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750213
Source datasetuspto-grants-1998_05
ORD IDord-4d15a69869384d4d8f3d83410bbca0cc
Source noteuspto-grants-1998_05