HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726506Generated: October 25, 2026
Tetrahydrofuran → HCID 178471409, compound
https://huagongshe.com/reaction/726506
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (3-(Ethoxycarbonyl)propyl)triphenylphosphonium Bromide | HCID 2773643 | — |
| Reactant | NaHMDS tetrahydrofuran | HCID 23700795 | — |
| Reactant | HCID 178520918 | HCID 178520918 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178471409 | HCID 178471409 | 62% |
Reaction Steps
First, 25.7 g of 3-ethoxycarbonylpropyltriphenylphosphonium bromide, 10.1 g of trans-4-(2,3-difluorophenyl)cyclohexanecarbaldehyde, and 150 ml of dry tetrahydrofuran were placed in a 300 ml flask. Then, 56.3 ml of 1.0M sodium bis(trimethylsilyl)amide/tetrahydrofuran solution was added dropwise to the reaction mixture at -70° C. to -60° C. The reaction mixture was stirred while being allowed to warm to room temperature over 6 hours. Ether was added to the reaction mixture. The ether solution 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: toluene/hexane=1/1) to obtain 9.0 g of 2,3-difluoro-1-[trans-4-(4-ethoxycarbonyl-1-butenyl)cyclohexyl]benzene (Y: 62%). The compound thus obtained had a purity of 89.2% (mixture of E and Z isomers) by GC.
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-5ce15233ac3344868d239d09bf7904c8 |
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| Source note | uspto-grants-1998_01 |
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