HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591012Generated: October 29, 2026
N-bromobutanimide → Methyl 2-(5-bromo-2-methyl-1,3-thiazol-4-yl)-2-(tert-butoxy)acetate
https://huagongshe.com/reaction/591012
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-(tert-butoxy)-2-(2-methyl-1,3-thiazol-4-yl)acetate | HCID 70819407 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(5-bromo-2-methyl-1,3-thiazol-4-yl)-2-(tert-butoxy)acetate | HCID 70819398 | — |
Reaction Steps
Under a nitrogen atmosphere, N-bromosuccinimide (39 mg, 0.22 mmol) was added to a solution of methyl 2-(tert-butoxy)-2-(2-methyl-1,3-thiazol-4-yl)acetate (15c) (50 mg, 0.21 mmol) in N,N-dimethylformamide (4 mL). The reaction mixture was warmed at 70° C. for 30 minutes then concentrated in vacuo. The residue was diluted with ethyl acetate (40 mL) and washed with water (2×20 mL), brine (20 mL), dried over sodium sulfate, filtered and evaporated under reduced pressure to give the desired product as a yellow oil without further purification (70 mg, 0.21 mmol, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238026B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-47fe65bfa4df4e749b86ed1184bd5ccd |
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| Source note | uspto-grants-2016_01 |
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