HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396403Generated: October 31, 2026
4-Methyl-5-(2-hydroxyethyl)thiazole → 103871-46-1
https://huagongshe.com/reaction/2396403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methyl-5-(2-hydroxyethyl)thiazole | HCID 1136 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 103871-46-1 | HCID 10935796 | 71.7% |
Reaction Steps
A solution of 5-(2-hydroxyethyl)-4-methylthiazole (306 g) and ethyl bromoacetate (356.2 g) in ethanol (1 L) was heated to reflux. After two hours, the ethanol was removed by distillation and the residue treated with isopropanol (1.5 L). The resulting solution was cooled to about 0° C., causing crystallization of compound 1. After three hours, the crystalline material was separated from the mother liquor. Additional crystals were obtained by prolonged cooling of the mother liquor at 0° C. Combination of the crystalline material gave 474.3 g of compound 1. Melting point 96°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05491241 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-2199beb11d7f418cb85e9ee5a0f469e2 |
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| Source note | uspto-grants-1996_02 |
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