HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296273Generated: November 1, 2026
Diethylamine → 4-bromo-N,N-diethyl-2-(trifluoromethoxy)benzamide
https://huagongshe.com/reaction/1296273
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Bromo-2-(trifluoromethoxy)iodobenzene | HCID 2736422 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 4-bromo-N,N-diethyl-2-(trifluoromethoxy)benzamide | HCID 68687835 | — |
Reaction Steps
To a stirring solution of 4-bromo-1-iodo-2-(trifluormethoxy)benzene (11600 mg, 32 mmol) in dry THF (300 mL) at −78° C. under Ar was added 2.5M n-butyllithium in hexanes (25 mL) dropwise. The reaction was stirred for 1.5 h and then quenched with crushed dry ice. The reaction was stirred for 30 min and then slowly wammed to room temperature. The reaction was partioned between 1 M hydrochloric acid in brine EtOAc. The organic layers were separated, washed with sat. aq. NaHSO3, dried over Na2SO4, and conc in vacuo to a brown oil. The oil was dissolved in dry CH2Cl2 (300 mL) with dry DMF (0.2 mL) and then treated with oxalyl chloride in CH2Cl2 (32 mL) dropwise. The reaction was stirred for 4 h and then conc in vacuo to a brown oil. The oil was dissolved in dry CH2Cl2 (300 mL) and then treated with diethylamine (5767 mg, 79 mmol) dropwise. The reaction was stirred for 48 h and then conc in vacuo to a brown oil. The oil was purified by flash chromatography (SiO2, 1:2, EtOAc:hexanes) to yield 8500 mg of the product as a colorless oil. MS (ESI) 341 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244843B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-7884ff7f006d4e0e976f7615260e1679 |
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| Source note | uspto-grants-2007_07 |
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