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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376629Generated: October 29, 2026

Diazomethane → HCID 53984498, compound

https://huagongshe.com/reaction/376629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 21195227HCID 21195227—
SolventDiethyl EtherHCID 3283—
ProductHCID 53984498HCID 5398449896%

Reaction Steps

A freshly prepared solution of diazomethane in anhydrous ether was added in excess to a solution of N-[2-(2-tert-butylphenylcarboxy)-1,1-dimethylethyl] trifluoromethanesulfonamide (13.1 g) in ether. The resulting yellow solution was allowed to stand at RT overnight, then was washed with 10% HCl followed by 2.5N aq NaOH. The organic solution was dried (MgSO4), and concentrated to afford 13.0 g of pure N-methyl-N-[2-(2-tert-butylphenylcarboxy)-1,1-dimethylethyl]-trifluoromethanesulfonamide as a white solid, a 96% yield. m.p. 42°-44° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE036562
Source datasetuspto-grants-2000_02
ORD IDord-1dc271f6e31a45db850a9cafde044af9
Source noteuspto-grants-2000_02