HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883216Generated: October 26, 2026
Dichloroacetyl chloride → 2,2-Dichloro-N-(3-ethynylphenyl) Acetamide
https://huagongshe.com/reaction/1883216
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenamine, 3-ethynyl- | HCID 104682 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Dichloro-N-(3-ethynylphenyl) Acetamide | HCID 2804962 | — |
Reaction Steps
3-Ethynylaniline (2.61 g, 22.3 mmol) was dissolved in anhydrous dichloromethane (20 mL) with triethylamine (3.1 mL, 22.3 mmol). The mixture was cooled in an ice-bath under nitrogen, then a solution of dichloroacetyl chloride (2.21 mL, 23 mmol) in anhydrous dichloromethane (20 mL) was added dropwise. After the addition was completed the ice-bath was removed and the mixture was stirred at room temperature for 2 h. The reaction mixture was then washed successively with water, 10% hydrochloric acid and saturated sodium bicarbonate solution. The organic solution was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the title compound as a beige solid (m.p. 99-100° C.). NMR (300 MHz, CDCl3): 8.05 (broad s, 1H, NH), 7.69 (s, 1H), 7.62 (m, 1H), 7.33 (m, 2H), 6.04 (s, 1H), 3.10 ppm (s, 1H, acetylenic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06759538B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-aa4f125ea8f94d21b2a5f95dd46b11e3 |
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| Source note | uspto-grants-2004_07 |
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