HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848749Generated: October 28, 2026
Pyridine → alpha-Chloro-alpha-(2,4-dichlorophenyl)-acetic acid t-butyl ester
https://huagongshe.com/reaction/848749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | alpha-Chloro-alpha-(2,4-dichlorophenyl)-acetyl chloride | HCID 20564372 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | alpha-Chloro-alpha-(2,4-dichlorophenyl)-acetic acid t-butyl ester | HCID 54191230 | 82.6% |
Reaction Steps
While stirring and with ice cooling, a solution of 17.6 g of t-butanol and 19.2 ml of pyridine in 60 ml of dichloromethane is dripped into a solution, cooled at 5° C., of 62 g of α-chloro-α-(2,4-dichlorophenyl)-acetyl chloride in 60 ml of dichloromethane in such a manner that the temperature of the reaction mixture stays below 10° C. After all the solution has been dripped in, the mixture is stirred overnight at room temperature, is then diluted with 100 ml of dichloromethane and extracted 5 times, each time with 100 ml of water. The organic phase is dried over magnesium sulfate and distilled after the solvent has been evaporated. There is obtained 58 g of α-chloro-α-(2,4-dichlorophenyl)-acetic acid t-butyl ester as a colorless oil; b.p. 98°-103° C./0.13 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04297364 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-f400aa52fe434e649fda6c635634b4cc |
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| Source note | uspto-grants-1981_10 |
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