HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910290Generated: October 28, 2026
Acetic Anhydride → 2-Acetamido-5-bromo-1,3-thiazole
https://huagongshe.com/reaction/910290
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Bromothiazol-2-amine monohydrobromide | HCID 2723848 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Acetamido-5-bromo-1,3-thiazole | HCID 350260 | — |
Reaction Steps
5.9 ml (42.3 mmol) of acetic anhydride are added to a solution of 10 g (38.5 mmol) of 2-amino-5-bromothiazole hydrobromide in 100 ml of dichloromethane and 11 ml (77 mmol) of triethylamine, cooled to 0° C. The reaction medium is stirred for 30 minutes at 0° C. and then for 18 hours at room temperature. After addition of water, the pH is adjusted to pH 8 with aqueous 1M sodium hydroxide solution and the reaction medium is extracted with dichloromethane. The dichloromethane phase is dried over magnesium sulfate, filtered and evaporated. The residue obtained is used in step b without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022079B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-4a25e5ee0d3d4512b0967e14f6614fc9 |
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| Source note | uspto-grants-2011_09 |
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