HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060240Generated: October 26, 2026
Potassium Carbonate → Tert-butyl 2-[(2-acetamido-1,3-thiazol-5-yl)sulfanyl]acetate
https://huagongshe.com/reaction/1060240
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | D-1,4-Dithiothreitol | HCID 446094 | — |
| Reactant | 2-Acetamino-5-thiocyanatothiazole | HCID 15346341 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 2-[(2-acetamido-1,3-thiazol-5-yl)sulfanyl]acetate | HCID 5329661 | 87% |
Reaction Steps
To a mixture of 2-acetamino-5-thiocyanatothiazole (5.97 g, 30 mmol) in MeOH (360 mL) under argon was added dithiothreitol (9.26 g, 60 mmol) at rt. The mixture was stirred at rt for 2 h and it was concentrated to afford a reduced solid product. This solid product was dissolved in DMF (30 mL) and to this solution were added tert-butyl bromoacetate (5.85 g, 30 mmol) and potassium carbonate (5.0 g, 36 mmol). The mixture was stirred at rt for 2 h and water (200 mL) was added to the mixture. The precipitates were collected, washed with water and dried. The solid was dissolved in methylene chloride (100 mL) and MeOH (10 mL) and filtered through a silica gel pad. The filtrate solution was concentrated to afford the desired product (7.5 g, 87%) as a solid, mp 162-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521759B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-3ef16d6a45dd47a595ca77d268693b4c |
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| Source note | uspto-grants-2003_02 |
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