HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (RS)-N-(4-Benzyloxy-phenyl)-2,4-dibromo-butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Benzyloxyaniline | HCID 22860 | — |
| Reactant | 2,4-Dibromobutyryl chloride | HCID 4413143 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (RS)-N-(4-Benzyloxy-phenyl)-2,4-dibromo-butyramide | HCID 23614762 | 22.2% |
Reaction Steps
A solution of 12.8 g (64.2 mmol) 4-benzyloxyaniline and 9.74 g (96.3 mmol) triethylamine in 125 ml dichloromethane is cooled to 0° C. 20.4 g (77.1 mmol) of 2,4-dibromobutyryl chloride [Ikuta et al., J. Med. Chem. 30:1995 (1987)] is slowly added over a period of 45 min. The reaction mixture is stirred for additional 15 min, then hydrolysed with 100 ml of water. The insoluble precipitate is filtered off and the organic phase is washed successively with a saturated solution of sodium hydrogencarbonate and water. After drying and evaporation, the crude product is subjected to chromatography (silica gel, dichloromethane) to yield 6.1 g (22%) of a colorless solid. Mp=139.5–142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235581B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-256f0b54b0f54f1f96eacf864eb6c106 |
| Source note | uspto-grants-2007_06 |