HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373735Generated: October 31, 2026
N,N-Dimethylaniline → N-[4-benzyloxy-2,6-bis(trifluoromethyl)phenyl]-2-bromoacetamide
https://huagongshe.com/reaction/1373735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 4-Benzyloxy-2,6-bis(trifluoromethyl)aniline | HCID 21075600 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[4-benzyloxy-2,6-bis(trifluoromethyl)phenyl]-2-bromoacetamide | HCID 21075603 | 64.7% |
Reaction Steps
Under an argon atmosphere, N,N-dimethylaniline (2.78 mL, 21.9 mmol) and bromoacetyl bromide (1.91 mL, 21.9 mmol) were added dropwise to a solution of 4-benzyloxy-2,6-bis(trifluoromethyl)aniline (4.90 g, 14.6 mmol) in anhydrous toluene (150 mL) under ice cooling. Immediately after the dropwise addition, the mixture was heated under reflux and then stirred for 1 hour. After cooling, the reaction mixture was filtered through Celite and the insoluble matter was washed with toluene. The residue obtained by distilling the filtrate under reduced pressure was purified by chromatography on a silica gel column (developing solvent; hexane:acetone=10:1→6:1→5:1). The crude product thus obtained was recrystallized from hexane-acetone, whereby 4.31 g (yield: 64.7%) of N-[4-benzyloxy-2,6-bis(trifluoromethyl)phenyl]-2-bromoacetamide was obtained as colorless needle-like crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163944B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-758d94ad5a20437e9bbeb57198c2ac0d |
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| Source note | uspto-grants-2007_01 |
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