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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889616Generated: October 30, 2026

N,O-Dimethylhydroxylamine → Benzophenone

https://huagongshe.com/reaction/1889616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,O-DimethylhydroxylamineHCID 14232—
ReactantHCID 178418255HCID 178418255—
ProductBenzophenoneHCID 3102—

Reaction Steps

The benzophenone derivative 70 was prepared using chemistry outlined in Scheme 13. Weinreb amide 69, derived via coupling of the acid chloride of the corresponding acid intermediate 62 with N,O-dimethylhydroxylamine, was treated with phenylmagnesium bromide to afford 70. Subsequent reduction of compound 70 with sodium borohydride provided alcohol 71, which was further reduced in the presence of trifluoroacetic acid to give the diphenylmethane derivative 72.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-62f03c75d5784fec9f63f067386856f0
Source noteuspto-grants-2013_08