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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362471Generated: October 31, 2026

HCID 57514173, compound → HCID 57514175, compound

https://huagongshe.com/reaction/2362471

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 numberUS08691831B2
Source datasetuspto-grants-2014_04
ORD IDord-a9f2d14011dc4bb1b56dd2991337f9cf
Source noteuspto-grants-2014_04