HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254941Generated: October 31, 2026
Hydrochloric Acid → HCID 178445614, compound
https://huagongshe.com/reaction/2254941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178445623 | HCID 178445623 | — |
| Product | HCID 178445614 | HCID 178445614 | 88.2% |
Reaction Steps
A mixture of 31 g (0.17 mol) of 2-(trans-4'-butylcyclohexyl) ethanol and 14 g (0.18 mol) of anhydrous pyridine was stirred over an ice water bath and 25 g (0.21 mol) of SOCl2 was added drop-wise to the mixture. The resulting reaction product was stirred and heated with a mantle heater at 105° to 110° C. for 3 hours. The reaction product was cooled to room temperature and poured into a beaker containing ice and concentrated hydrochloric acid. The oily layer was separated out and the aqueous layer was extracted with chloroform. The two layer were combined and washed with an aqueous 10% hydrochloric acid solution and water. The chloroform was distilled off. The residual liquid was distilled in a vacuum (b.p. 96° C./3 mmHg) to yield 30 g (0.15 mol) of 2-(trans-4'-butylcyclohexyl)-1-chloroethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05238599 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-4da57811106d4495b6bc9dfaebbbb1f6 |
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| Source note | uspto-grants-1993_08 |
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