HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247782Generated: October 25, 2026
Chloride → Benzoic acid, 4-(phenylmethoxy)-, 1-(trifluoromethyl)nonyl ester
https://huagongshe.com/reaction/247782
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 4-Benzyloxybenzoylchloride | HCID 3766410 | — |
| Reactant | 1,1,1-Trifluorodecan-2-ol | HCID 3864464 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Benzoic acid, 4-(phenylmethoxy)-, 1-(trifluoromethyl)nonyl ester | HCID 14745753 | 96.3% |
Reaction Steps
To a solution of 4-benzyloxybenzoic acid chloride (1.23 g) in methylene chloride (10 ml) was slowly added under ice cooling a solution of optically active 1,1,1-trifluoro-2-decanol (0.96 g), dimethylaminopyridine (0.55 g) and triethylamine (0.48 g) in methylane chloride (20 ml). The mixture was left to stand until it reached room temperature and allowed to react overnight. The mixture was poured in ice water and extracted with methylene chloride. The extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water in this order, and was dried over anhydrous magnesium sulfate. After the solution was distilled to remove the solvent, the crude product thus obtained was purified by toluene-silica-gel column chromatography and recrystallized from ethanol to obtain the titled compound (1.84 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05207947 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-859e072770fa41648e889dcb531ae8cb |
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| Source note | uspto-grants-1993_05 |
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