HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707535Generated: October 30, 2026
Hydrochloric Acid → HCID 178445623, compound
https://huagongshe.com/reaction/1707535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 178445626 | HCID 178445626 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178445623 | HCID 178445623 | 89.5% |
Reaction Steps
37 g (0.19 mol) of trans-4-butylcyclohexyl acetic acid was dispersed in 190 cm) of anhydrous toluene, 160 cm3 (0.57 mol) of 70% of NaAlH2 (OC2H4OCH3)2 in toluene was added dropwise while stirring at a rate where the toluene refluxed quietly, after which it was stirred for 3 hours on a 90° C. hot water bath. The reactant was cooled to room temperature, 40 cm3 of water and 500 cm3 of 15% HCl were added dropwise while stirring, the oily layer was taken off, and the water layer was extracted with toluene, combined with the oily layer and washed with 10% HCl and water. The toluene was removed, and the remaining oily substance was distilled under reduced pressure (b. p. 103° C./3 mmHg) to obtain 31 g (0.17 mol) of 2-(trans-4'-butylcyclohexyl)ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05354502 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-c1e6c4ca22694117b0f929bab46a130e |
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| Source note | uspto-grants-1994_10 |
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