HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dichloroacetone → tert-Butyl (4-(chloromethyl)thiazol-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-Boc thiourea | HCID 4095660 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | tert-Butyl (4-(chloromethyl)thiazol-2-yl)carbamate | HCID 45117840 | 68.2% |
Reaction Steps
To a solution of N-Boc-thiourea (3.0 g, 17 mmol) in acetone (75 mL) was added 1,3-dichloroacetone (2.4 g, 18.7 mmol) at once. The mixture was stirred at room temperature for 72 h. The reaction mixture was treated with 3 g of NaHCO3 and stirred for 15 min. The solids were removed by filtration and the filtrate was concentrated in vacuo. Column chromatography (EtOAc/Heptanes 4/1) afforded N-Boc-4-(chloromethyl)thiazol-2-amine (2.9 g, 11.6 mmol, 68%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148380B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-c2ac4b517c1941708f18ba4abfb8e6d8 |
| Source note | uspto-grants-2012_04 |