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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methoxyacetone | HCID 22172 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(Methoxymethyl)-1,3-thiazol-2-amine | HCID 23092527 | 33% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514566B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-6812f5879b00413b99c14227fc5f2a88 |
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| Source note | uspto-grants-2009_04 |
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