HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (S)-6-(4-bromophenyl)-1,4-oxazepane hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | (S)-6-(4-bromophenyl)-4-((R)-1-phenylethyl)-[1,4]oxazepane | HCID 67281235 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | (S)-6-(4-bromophenyl)-1,4-oxazepane hydrochloride | HCID 66718622 | 86% |
Reaction Steps
To a solution of (S)-6-(4-bromophenyl)-4-((R)-1-phenylethyl)-[1,4]oxazepane (0.610 g, 1.69 mmol) in 1,2-dichloroethane (2.83 ml) was added 1-chloroethyl chloroformate (0.605 g, 4.23 mmol) at room temperature. The mixture was refluxed for 4 hours and cooled to room temperature. After addition of methanol (5.0 ml), the mixture was refluxed for 3 hours and concentrated under reduced pressure to afford the crude product. This crude product was washed with ether, dried under reduced pressure to afford (S)-6-(4-bromophenyl)-1,4-oxazepane hydrochloride as white solid (0.424 g, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108957B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-e4d26c374edc467098608dcbc572e5a1 |
| Source note | uspto-grants-2015_08 |