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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977353Generated: October 25, 2026

N-methylhydroxylamine hydrochloride → 3-(N-methyl-hydroxycarbamoyl)-5-nitro-benzoic acid allyl ester

https://huagongshe.com/reaction/1977353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methylhydroxylamine hydrochlorideHCID 77906—
Reactant5-Nitro-isophthalic acid 1-(2,5-dioxo-pyrrolidin-1-yl) ester 3-allyl esterHCID 22986099—
SolventDichloromethaneHCID 6344—
Product3-(N-methyl-hydroxycarbamoyl)-5-nitro-benzoic acid allyl esterHCID 2298610188.9%

Reaction Steps

Starting material (8(c)) was prepared as follows. A mixture of 7(b) (2.00 g; see Example 7), N-methylhydroxylamine hydrochloride (1.06 g) triethylamine (1.72 ml) and dichloromethane (60 ml.) was stirred at 5° or 30 minutes. It was then allowed to warm to ambient temperature and stirred for a further 16 hours. The reaction mixture was then poured directly onto a flash column eluting with ethyl acetate/hexane (50:50) to give 3-(N-methyl-hydroxycarbamoyl)-5-nitro-benzoic acid allyl ester (8(a)) as a cream solid (1.43 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232338B1
Source datasetuspto-grants-2001_05
ORD IDord-8eaf5aa4cfe0494f8a6de93fa605939b
Source noteuspto-grants-2001_05