HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050171Generated: October 30, 2026
Thionyl Chloride → 2-Hydroxy-N-(1,2,2,2-tetrachloroethyl)benzamide
https://huagongshe.com/reaction/2050171
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2674-50-2 | HCID 232983 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Hydroxy-N-(1,2,2,2-tetrachloroethyl)benzamide | HCID 12940170 | — |
Reaction Steps
2,500 ml of benzene was added to 1,423 g of N-(1'-hydroxy-2',2',2'-trichloroethyl)-2-hydroxy benzamide and then 833 g of thionyl chloride was added thereto and heated under reflux at 70°-80° C. for 4 hours to obtain N-(1',2',2',2'-tetrachloroethyl)-2-hydroxy benzamide (white crystal, melting point of 113°-113.5° C., Anal. Found: C,35.74; H,2.12; N,4.70 Calcd. for C9H7Cl4NO2 : C,35.68; H,2.33; N,4.62 and the resultant reaction mixture, without separation of the crystals, was cooled to below 30° C. and mixed with 1,250 g of methanol and heated under reflux for 2 hours at 55°-60° C. followed by removing the solvent and the residue was poured into water, filtered and dried to obtain 1,380 g (yield 92.4%) white crystals of N-(1'-methoxy-2',2',2'-trichloroethyl)-2-hydroxy benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04200632 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-59dbc18478c14be69b91dd55cabaec81 |
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| Source note | uspto-grants-1980_04 |
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