HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181403Generated: November 3, 2026
Hydrochloric Acid → (3-(Chlorocarbonyl)-2-methylphenyl)acetate
https://huagongshe.com/reaction/2181403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Acetoxy-2-methylbenzoic acid | HCID 3798557 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | (3-(Chlorocarbonyl)-2-methylphenyl)acetate | HCID 7010345 | 97.3% |
Reaction Steps
In a flask, 60.0 g of 3-acetoxy-2-methylbenzoic acid are suspended under nitrogen in 140.0 g of xylene. The suspension is heated to 70° C. and 42.9 g of thionyl chloride are added dropwise. The mixture is heated further. At approx. 75° C., vigorous gas evolution (SO2, HCl) commences. The liquid phase temperature rises continuously and reaches 108° C. after approx. 4 h. The solution is cooled to approx. 50° C. under nitrogen and the reflux condenser is replaced by Vigreux column. At atmospheric pressure and later under reduced pressure, first xylene and thionyl chloride residues and then the product are distilled over. The product distills over at 15 mbar and 147.0-148.0° C. 59.6 g of 3-acetoxy-2-methylbenzoyl chloride (97.3%) are obtained. This corresponds to 91.0% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06891060B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-d67a096240fb4e09b213bad8477b1b83 |
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| Source note | uspto-grants-2005_05 |
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