HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282445Generated: October 31, 2026
Chloroacetyl chloride → HCID 23513422, compound
https://huagongshe.com/reaction/1282445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-5-methylphenol | HCID 76082 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23513422 | HCID 23513422 | 74% |
Reaction Steps
95 ml of triethylamine (0.674 mol) were added to a solution of 83 g of 2-hydroxy-4-methylaniline (0.674 mol) in 2.5 liters of tetrahydrofuran, with stirring and under an inert atmosphere, followed, after 30 minutes, by dropwise addition of a solution of 54 ml of chloroacetyl chloride (0.678 mol) in 60 ml of tetrahydrofuran, while maintaining the temperature at 25-27° C. The reaction medium was stirred at room temperature for 4 hours, filtered through a sinter funnel and the inorganic salts were rinsed with 500 ml of tetrahydrofuran. The combined organic phases were poured into 3 liters of ice-cold water with stirring. The precipitate formed was spin-filtered, washed with twice 600 ml of water and once with pentane, and dried under vacuum to constant weight, to give 99 g of 2-chloro-N-(2-hydroxy-4-methylphenyl)acetamide in the form of a beige-coloured powder, in a yield of 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455737B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-ef1c25e2a3244a33b006289dcb19e83b |
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| Source note | uspto-grants-2002_09 |
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