HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762022Generated: October 30, 2026
HCID 13463460, compound → HCID 178444426, compound
https://huagongshe.com/reaction/1762022
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13463460 | HCID 13463460 | — |
| Reactant | HCID 178444415 | HCID 178444415 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178444426 | HCID 178444426 | — |
Reaction Steps
The crude (S)-4-(6-methyloctyloxy)benzoyl chloride obtained was dissolved in 20 ml of toluene and then added dropwise to a solution of 0.26 g of 4-[2-(trans-4-pentylcyclohexyl)ethyl]phenol in 2 ml of pyridine. The reaction mixture was stirred at room temperature overnight, then poured into ice-water and extracted with diethyl ether. The extract was washed four times with 25 ml of 1N hydrochloric acid each time, then washed with 25 ml of 2N sodium carbonate solution and several times with water, dried over magnesium sulphate and concentrated. Chromatography of the residual oil on silica gel with toluene gave 0.2 g of (S)-4-(6-methyloctyloxy)benzoic acid 4-[2-(trans-4-pentylcyclohexyl)ethyl]phenyl ester. The product was recrystallized several times from ethanol until the phase transition temperatures were constant. M.p. (C-S) 58°, transition S-S*C 58.5° C., transition S*C -Ch 93° C., cl.p. (CH-I) 140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04830470 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-17dcfdb9a7a7420198e6915af56c14fe |
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| Source note | uspto-grants-1989_05 |
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