HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726510Generated: October 30, 2026
Tetrahydrofuran → HCID 178460515, compound
https://huagongshe.com/reaction/726510
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | HCID 178521549 | HCID 178521549 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178460515 | HCID 178460515 | 52.6% |
Reaction Steps
First, 4.24 g of trans-4-(2,3-difluorophenyl)cyclohexanol, 2 g of triethylamine, and 60 ml of tetrahydrofuran were placed in a 100 ml flask. Then, 2.3 g of acryloyl chloride was added dropwise to the mixture under ice water cooling. The mixture was stirred at the same temperature for 3 hours. Water was added to the reaction mixture, and an organic layer was extracted with ether. The ether layer was washed with water and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: benzene/hexane=1/1) and recrystallized from hexane to obtain 2.8 g of trans-4-(2,3-difluorophenyl)cyclohexyl acrylate (Y: 52.6%). The compound thus obtained had a purity of 99.9% by GC and 99.5% by HPLC. Furthermore, the compound had an m.p. of 72.9° C. to 73.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05709911 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-5987429c551945a099f57d037f81d7dd |
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| Source note | uspto-grants-1998_01 |
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