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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 2,3-Difluoro-4'-[12,12-bis(hydroxymethyl)dodecyl]oxybiphenyl | HCID 18920846 | — |
| Product | 2,3-Difluoro-4'-[12,12-bis(acryloyloxymethyl)dodecyl]oxybiphenyl | HCID 18920868 | 57% |
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
| 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-555dcde752ec4a2593cb9152ed174dc0 |
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| Source note | uspto-grants-1998_05 |
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