HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418353Generated: October 30, 2026
N-bromobutanimide → 2-(2-Amino-1,3-thiazol-5-yl)ethan-1-ol
https://huagongshe.com/reaction/418353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Amino-1,3-thiazol-5-yl)ethan-1-ol | HCID 13637184 | 117.5% |
Reaction Steps
To an ice cold suspension of NBS (1.182 g, 6.72 mmol) in water (8 mL) was added 2,3-dihyofuran (0.75 mL, 9.92 mmol) slowly. The resulting solution was stirred at 0° C. for 1 h, followed by addition of thiourea (0.505 g, 6.63 mmol). The mixture was heated under reflux under nitrogen atmosphere overnight to form a yellow clear solution. The mixture was extracted with EtOAc (3×5 mL) and the aqueous solution was treated with ammonium hydroxide to pH 12. The solution was extracted with CH2Cl2 (2×5 mL), followed by extraction with EtOAc (8×10 mL). The CH2Cl2 layer contains small amount of product and large amount of impurities, which was discarded. The EtOAc layers were combined, dried, and concentrated to give 1.123 g 2-(2-amino-thiazol-5-yl)-ethanol
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093266B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-48bc12f0657a4999a7d5c88dc76e13c4 |
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| Source note | uspto-grants-2012_01 |
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