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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 11-[2,3-Difluorobiphenyl-4'-yl]oxyundecyl 2,2-bis(6-hydroxyhexyl)acetate | HCID 18920835 | — |
| Product | 11-[2,3Difluorobiphenyl-4'-yl]oxyundecyl 2,2-bis(6-acryloyloxyhexyl)acetate | HCID 18920849 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05750213 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-01897ce5ef054f13a88ecc58e7b9cf9e |
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| Source note | uspto-grants-1998_05 |
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