HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569177Generated: October 27, 2026
Methyl Acetate → 3-[p-(3-Acetoxy-1-chloro-2-methylpropyl)benzyl]pyridine
https://huagongshe.com/reaction/569177
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Acetate | HCID 6584 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-[p-(3-Acetoxy-1-hydroxy-2-methylpropyl)benzyl]pyridine | HCID 20148636 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[p-(3-Acetoxy-1-chloro-2-methylpropyl)benzyl]pyridine | HCID 13745528 | 86% |
Reaction Steps
In 4.6 ml of methylene chloride was dissolved 910 mg of 3-[p-(3-acetoxy-1-hydroxy-2-methylpropyl)benzyl]pyridine, and to the resulting solution was added 0.48 ml of thionyl chloride with ice-cooling, after which the resulting mixture was subjected to reaction at the same temperature for one hour. The solvent and the excessive thionyl chloride were removed by distillation under reduced pressure, and to the residue thus obtained were added 10 ml of methyl acetate and 10 ml of water, after which the resulting mixture was neutralized with sodium hydrogencarbonate. The organic layer was separated, washed with 5 ml of water, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and the residue thus obtained was purified by a column chromatography [Wako Silica Gel C-200, eluant: benzene:ethyl acetate (5:1 by volume)] to obtain 740 mg (yield 86.0%) of colorless, oily 3-[p-(3-acetoxy-1-chloro-2-methylpropyl)benzyl]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04731370 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-7962bbd87b844780b3401364221aeb4e |
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| Source note | uspto-grants-1988_03 |
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