HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647034Generated: October 30, 2026
Hydrochloric Acid → HCID 12906128, compound
https://huagongshe.com/reaction/647034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3,5-Trimethylphenol | HCID 12769 | — |
| Reactant | Hexanoic acid, 6-chloro-6-oxo-, ethyl ester | HCID 14065 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,1,1,2-Tetrachloroethane | HCID 12418 | — |
| Product | HCID 12906128 | HCID 12906128 | — |
Reaction Steps
To a solution of 2,3,5-trimethylphenol(formula VII wherein R=H3C, X=H, Y=OH) (1.4 part) in tetrachloroethane (10 volume parts), there was added a solution of aluminum chloride dust (3.5 parts) and ethyl 5-chloroformylpentanoate (3 parts) in tetrachloroethane (5 volume parts) at 0° C. and in a current of nitrogen gas and the mixture was heated at 110°-120° C. for 17 hours. To the reaction mixture was added cold water (50 volume parts) and the dilution was acidified with dilute hydrochloric acid and extracted with chloroform (200 volume parts). The residue (2.7 parts) obtained from the extract was subjected to column chromatography on silicic acid (60 parts) and eluted with chloroform-diethyl ether (20:1) (300 volume parts). The eluate was evaporated to dryness and the residue was recrystallized from ethanol. The procedure provided colorless needles of ethyl 5-(2'-hydroxyl-3',4',6'-trimethylbenzoyl)pentanoate (formula II-1 wherein R=H3C, X=H, Y=OH, n=4, in the form of ethyl ester) (1.9 part) melting at 72°-73° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04407757 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-12e1d27fb51f4243bfa64c62b77a76a3 |
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| Source note | uspto-grants-1983_10 |
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