HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259721Generated: October 28, 2026
Triethylamine → 2-Amino-3-benzoyl-5-chloro-α-(methylthio)benzeneacetamide
https://huagongshe.com/reaction/2259721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-5-chlorobenzophenone | HCID 12870 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Reactant | 2-(Methylthio)acetamide | HCID 547873 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Amino-3-benzoyl-5-chloro-α-(methylthio)benzeneacetamide | HCID 67079956 | — |
Reaction Steps
To a cold (-70° C.) solution of 12.77 g (0.055 mole) of 2-amino-5-chlorobenzophenone in 300 mL of methylene chloride, under nitrogen atmosphere, was added 6.0 g (0.552 mole) of t-butylhypochlorite in 20 mL of methylene chloride. After the reaction was stirred for an additional 15 min, a suspension of 5.8 g (0.055 mole) of α-(methylthio)acetamide in 150 mL of methylene chloride was added. The mixture was stirred at -65° C. for 1 h. Triethylamine (5.6 g, 0.055 mole) was added and the solution was allowed to warm to room temperature. The reaction mixture was extracted with water and the organic layer dried over magnesium sulfate. The volume of the solution was reduced in vacuo to about 200 mL and the product crystallized as a yellow solid, m.p. 173.5°-174.5° C. Yield was 6.86 g (37.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05475034 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-a425f2e364eb4008be119daaabf0d083 |
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| Source note | uspto-grants-1995_12 |
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