HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897624Generated: October 30, 2026
Diisopropylethylamine → HCID 22347194, compound
https://huagongshe.com/reaction/897624
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 2-(4-Bromoanilino)-1-phenylethan-1-ol | HCID 13351411 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22347194 | HCID 22347194 | 151.2% |
Reaction Steps
A solution containing 2-(4-bromoanilino)-1-phenyl-1-ethanol (0.74 g, 0.00253 mol), N,N-diisopropylethylamine (1.01 g, 0.00786 mol) and N,N-dimethylaminopyridine (0.092 g, 0.00076 mol) in anhydrous dichloromethane (32 mL) was cooled to 0° C. and a solution of triphosgene (0.38 g, 0.00127 mol) in anhydrous dichloromethane (8 mL) was added dropwise. The reaction mixture was slowly warmed up to ambient temperature while stirring under an atmosphere of nitrogen for eighteen hours. The organic phase was washed with a saturated solution of sodium bicarbonate in water (40 mL), brine (30 mL) and dried with magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by flash chromatography on silica using ethyl acetate/n-heptane (1:5) as mobile phase to yield 3-(4-bromophenyl)-5-phenyl-1,3-oxazolan-2-one (0.62 g, 0.00192 mol) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06921763B2 |
|---|
| Source dataset | uspto-grants-2005_07 |
|---|
| ORD ID | ord-50c518ad296a498db7e5e615cec415ca |
|---|
| Source note | uspto-grants-2005_07 |
|---|