HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → HCID 21072848, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phenacylamine | HCID 11952 | — |
| Reactant | 2-(2-aminophenyl)propan-2-ol | HCID 253527 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Product | HCID 21072848 | HCID 21072848 | — |
Reaction Steps
112 g (1.13 mol) of phosgene are piped into 500 mL of THF. Then a solution of 52 g (0.34 mol) of 2-(2-aminophenyl)propan-2-ol, prepared from 2-aminoacetophenone and methylmagnesium iodide, in 300 mL of THF is added. The reaction mixture is left to stand overnight, evaporated down, and combined with 500 mL of pyridine. After the pyridine has been distilled off, water is added and the mixture is extracted with diethyl ether. The organic phases are washed successively with 2 N hydrochloric acid, sodium hydroxide solution and water, dried with sodium sulfate, and evaporated down. The residue remaining (46 g) is further reacted directly without any more purification. M.p. (toluene/petroleum ether)=109° C.-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632834B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-86de510f7e5e4f1bb5d21997b6bc9454 |
| Source note | uspto-grants-2009_12 |