HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164677Generated: October 31, 2026
N,N-Dimethylaniline → HCID 21286895, compound
https://huagongshe.com/reaction/2164677
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 2-Amino-4-chlorophenol | HCID 7265 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 21286895 | HCID 21286895 | 52.6% |
Reaction Steps
To a mixture of 2-amino-4-chlorophenol (19.50 g.) and N,N-dimethylaniline (19.90 g.) in dry acetone (200 ml.) was added dropwise bromoacetyl bromide (33.2 g.) over a period of 15 minutes under ice-cooling at below 10° C. with stirring and stirring was continued for 45 minutes at the same temperature. The reaction mixture was evaporated and to the residue were added ethyl acetate and water. The ethyl acetate layer was washed with 5% hydrochloric acid (twice), water, 5% aqueous solution of sodium bicarbonate, water (twice) and a saturated aqueous solution of sodium chloride successively, dried over magnesium sulfate, treated with activated charcoal and then evaporated. The residue was recrystallized from a mixture of ethyl acetate and diisopropyl ether to give the title compound (18.91 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04506076 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-f48708a66f7048ff9ffc6da48abbac24 |
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| Source note | uspto-grants-1985_03 |
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