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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73261Generated: October 28, 2026

HCID 57514173, compound → HCID 57514175, compound

https://huagongshe.com/reaction/73261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57514173HCID 57514173—
SolventEthyl AcetateHCID 8857—
ProductHCID 57514175HCID 5751417566.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829036B2
Source datasetuspto-grants-2014_09
ORD IDord-d225351ebd244a7db19ecb4cb38ce393
Source noteuspto-grants-2014_09