HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656258Generated: November 2, 2026
N,N-Dimethylaniline → 4-Nitrobenzyl bromoacetate
https://huagongshe.com/reaction/1656258
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 4-Nitrobenzyl alcohol | HCID 69275 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | 4-Nitrobenzyl bromoacetate | HCID 7015321 | — |
Reaction Steps
To a mixture of p-nitrobenzyl alcohol (45 g) and N,N-dimethylaniline (37.2 ml) in a mixture of diisopropyl ether and diethyl ether (300 ml) was added dropwise bromoacetyl bromide (25 ml) at 30° to 35° C., and the reaction mixture was stirred at the same temperature for an hour. After the reaction mixture was poured into ice-water, the separated organic layer was washed with 5% aqueous sodium bicarbonate. The solution was evaporated under reduced pressure to give p-nitrobenzyl bromoacetate. To a solution of this residue in N,N-dimethylformamide (150 ml) was added N-hydroxyphthalimide 39.3 g) and triethylamine (50 ml), and the reaction mixture was stirred for an hour at room temperature. The resultant mixture was poured into ice-water, and the precipitates were collected by filtration and washed with water to give p-nitrobenzyl 2-phthalimidooxyacetate (69.26 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05252731 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-4b2ee7ca7779417bac2b7768b1813c82 |
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| Source note | uspto-grants-1993_10 |
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