HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198839Generated: October 30, 2026
Hydrochloric Acid → HCID 178491465, compound
https://huagongshe.com/reaction/1198839
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 178491466 | HCID 178491466 | — |
| Product | HCID 178491465 | HCID 178491465 | — |
Reaction Steps
A solution of 16.3 g of p-[trans-4-(p-anisyloxymethyl)-cyclohexyl]benzoyl chloride in 50 ml of dichloroethane is cooled to 7° C. and treated portionwise under nitrogen within 5 minutes with 6.4 g of powdered aluminium chloride. A weak stream of acetylene gas is then conducted through the reaction mixture at 45° C. for 17 hours. The reaction mixture is subsequently poured into 100 ml of ice-water, treated with 50 ml of 3N hydrochloric acid and stirred for 10 minutes. The mixture is extracted with diethyl ether. The organic phase is washed in succession with water, with 5 percent potassium hydroxide solution and several times with water, then dried over magnesium sulphate and evaporated. The trans-4-(p-anisyloxymethyl)-1-[p-(3-chloroacryloyl)phenyl]cyclohexane obtained is purified by chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04898455 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-968446f175f04488a3ddecd60f3eef6d |
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| Source note | uspto-grants-1990_02 |
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