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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825273Generated: November 2, 2026

Diazomethane → HCID 72509424, compound

https://huagongshe.com/reaction/1825273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 22145275HCID 22145275—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 72509424HCID 7250942472.1%

Reaction Steps

A solution of 3-(2-ethylphenyl)propanoyl chloride (crude, 23.8 mmole) in methylene chloride was slowly added to a solution of diazomethane (generated from 15.6 g of 1-methyl-3-nitro-1-nitrosoguanidine) in ether (100 ml) cooled in an ice bath. The mixture was then warmed up to room temperature and stirred overnight. The mixture was concentrated in vacuo and purified by column chromatography (10→20% ethyl acetate/hexanes) to give 1-diazo-4-(2-ethylphenyl)butan-2-one (3.47 g, 72% over 2 steps). 1H NMR (CDCl3) δ 7.1-7.25 (4H, m, phenyl), 5.21 (1H, broad s, diazo), 2.97 (2H, m, CH2 of ethyl), 1.20 (3H, t, CH3). Step 3:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045591B2
Source datasetuspto-grants-2006_05
ORD IDord-f62fc180b76a4c81a2034e108bd00655
Source noteuspto-grants-2006_05