HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloroacetyl chloride → 2,2-Dichloro-N-(4-ethynylphenyl)Acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Ethynylaniline | HCID 3760025 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Dichloro-N-(4-ethynylphenyl)Acetamide | HCID 21100338 | — |
Reaction Steps
4-Ethynylaniline (2.94 g, 25.1 mmol) was dissolved in anhydrous dichloromethane (20 mL) with triethylamine (4.55 mL, 32.6 mmol). The mixture was cooled in an ice-bath under nitrogen, then a solution of dichloroacetyl chloride (2.42 mL, 25.1 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 12 h. The reaction mixture was then washed successively with water, 20% 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 brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07326790B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-428fdc1cbd7048e6a64728bd42414146 |
| Source note | uspto-grants-2008_02 |