HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 57514173, compound → HCID 57514175, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 57514173 | HCID 57514173 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57514175 | HCID 57514175 | 66.2% |
Reaction Steps
To a solution of tert-butyl 2-(3-bromophenyl)-1-hydroxypropan-2-ylcarbamate (CD1; R4=Me) (1.5 g, 4.6 mmol) in EtOAc (150 mL) at reflux was added IBX (3.82 g, 13.6 mmol, 3 eq). Reflux was continued for another 2 h and then the mixture was cooled to RT. The white precipitate was filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel by eluting with EtOAc/hexanes to give 1.0 g (66%) of tert-butyl 2-(3-bromophenyl)-1-oxopropan-2-ylcarbamate (CD2; R4=Me) as a colorless oil. 1H NMR (CDCl3) δ 9.42 (s, 1H), 7.69 (m, 1H), 7.60 (m, 1H), 7.55-7.40 (m, 2H), 5.85 (bs, 1H), 1.96 (s, 3H), 1.56 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829036B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-d225351ebd244a7db19ecb4cb38ce393 |
| Source note | uspto-grants-2014_09 |