Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109724Generated: October 31, 2026

Methoxyacetone → 4-(Methoxymethyl)-1,3-thiazol-2-amine

https://huagongshe.com/reaction/2109724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetoneHCID 22172—
ReactantBromineHCID 24408—
ReactantThioureaHCID 2723790—
SolventMethanolHCID 887—
Product4-(Methoxymethyl)-1,3-thiazol-2-amineHCID 2309252733%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1-methoxypropan-2-one (20.3 g, 231 mmol) in 200 mL of MeOH was added to a 250 mL round-bottom flask. The flask was then immersed in an ice-water bath. Br2 was added dropwise to the reaction mixture through an addition funnel. After the addition, the addition funnel was rinsed with 50 mL MeOH, and the reaction mixture was stirred for 20 minutes at 0° C. The ice-water bath was then removed, and the reaction mixture was stirred for two more hours. Thiourea (18 g, 231 mmol) was then added to the reaction mixture, and the reaction was heated at reflux overnight. The reaction was concentrated, and saturated sodium bicarbonate and solid sodium carbonate were used to adjust the pH to 8-9. The resulting mixture was then extracted three times with 200 mL portions of EtOAc. The organic layers were concentrated and then purified by recrystallization to give 4-(methoxymethyl)thiazol-2-amine (11 g, 33% yield over two steps). MS m/z: 145 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514566B2
Source datasetuspto-grants-2009_04
ORD IDord-6812f5879b00413b99c14227fc5f2a88
Source noteuspto-grants-2009_04