HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848058Generated: November 2, 2026
Carbon Tetrachloride → 2-Hydroxy-N-(1,2,2,2-tetrachloroethyl)benzamide
https://huagongshe.com/reaction/848058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2674-50-2 | HCID 232983 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Hydroxy-N-(1,2,2,2-tetrachloroethyl)benzamide | HCID 12940170 | — |
Reaction Steps
5 g of thionyl chloride was added dropwise to the mixture of 10 g of N-(1-hydroxy-2,2,2-trichloroethyl)-2-hydroxybenzamide, 50 ml of carbon tetrachloride and 0.1 g of N,N-dimethylformamide under stirring. After effecting the reaction under reflux for one hour, the solvent was distilled off under reduced pressure to obtain N-(1,2,2,2-tetrachloroethyl)-2-hydroxybenzamide (m.p.: 113°-113.5° C.). Without taking out the compound thus resulted, thereto were added 50 ml of acetone and also 7.2 g of octyl thioglycolate (n), and the mixture was stirred at room temperature for one hour. The solvent was distilled off and the rest was purified by silica gel column chromatography to obtain 3.0 g of N-(1-n-octyloxycarbonylmethylthio-2,2,2-trichloroethyl)-2-hydroxybenzamide as a light yellow oily substance. nD25 1.5031
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04294835 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-4499cafb62364ccaa8c067aaf3ca182b |
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| Source note | uspto-grants-1981_10 |
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