HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728749Generated: October 26, 2026
Phenacyl bromide → Phenacyl 3-hydroxy-2-n-tetradecyl-11-icosenoate
https://huagongshe.com/reaction/728749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Hydroxy-2-n-tetradecyl-11-icosenoic acid | HCID 53940126 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenacyl 3-hydroxy-2-n-tetradecyl-11-icosenoate | HCID 53739963 | 22.1% |
Reaction Steps
3-Hydroxy-2-n-tetradecyl-11-icosenoic acid (II)(3.68 g, 7.04 millimole) was dissolved in dry tetrahydrofuran (100 ml), and phenacyl bromide (2.10 g, 10.56 millimole) and triethyl amine (1.47 ml, 10.56 millimole) were successively added thereto with ice cooling. The reaction mixture was allowed to warm to room temperature, and to react for 13.5 hours. The insoluble matter in the reaction mixture was filtered off with suction and the solvent was distilled off from the filtrate. The residue was dissolved in methylene chloride and the obtained solution was successively washed with water and saturated aqueous sodium chloride solution, and dried over anhydrous sodium sulfate. The inorganic salt was filtered off and the solvent was distilled off from the filtrate. The obtained residue was purified over a silicagel column (benzene -→ benzene:ethyl acetate=8:2) to give phenacyl 3-hydroxy-2-n-tetradecyl-11-icosenoate (IV)(998.6 mg, yield 22.1%) in the form of white viscous solid. IR(νmaxKBr, cm-1); 3340, 2900, 2850, 1740, 1705
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05049664 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-2df9f322f0c24fca9dd6ee783b2e70b2 |
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| Source note | uspto-grants-1991_09 |
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