Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941471Generated: October 25, 2026

N-Benzyl-N-nitroso-p-toluenesulfonamide → Benzene, (diazomethyl)-

https://huagongshe.com/reaction/1941471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Benzyl-N-nitroso-p-toluenesulfonamideHCID 4118076—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Solventtert-Butyl methyl etherHCID 15413—
ProductBenzene, (diazomethyl)-HCID 13660130%

Reaction Steps

N-Nitroso-N-benzyl-p-toluene sulphonamide (966 mg, 3.33 mmol) was added in small portions to a solution of sodium methoxide (2.0 ml of 2M solution in methanol) in t-butyl methyl ether (12 ml) and methanol (2 ml) at room temperature. After the addition was finished the reaction mixture was refluxed for 15-30 min. The reaction mixture was cooled and washed with water (3×6 ml). The ethereal solution of phenyl diazomethane was dried over sodium sulphate for 30 minutes. The solvent was removed in vacuo and the residue distilled under reduce pressure to give phenyl diazomethane as a dark red oil (30% yield, b.p. 20° C. at 1 mmHg) which was immediately dissolved in t-butyl methyl ether (6 ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703246
Source datasetuspto-grants-1997_12
ORD IDord-f49d6f158adc41dfba6332ceeb0af4e9
Source noteuspto-grants-1997_12