HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → (2-Acetamido-5-bromothiazol-4-yl)methyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | (2-Acetamido-1,3-thiazol-4-yl)methyl acetate | HCID 14931747 | — |
| Reactant | (2-acetamidothiazol-4-yl)methyl acetate AcOH | HCID 86613765 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (2-Acetamido-5-bromothiazol-4-yl)methyl acetate | HCID 57633964 | 81.2% |
Reaction Steps
(2-Acetamidothiazol-4-yl)methyl acetate (9.00 g, 42 mmol) was dissolved in 30 mL AcOH. A mixture of Br2 (9.0 g, 56.7 mmol) in 20 mL AcOH was added dropwise to the (2-acetamidothiazol-4-yl)methyl acetate/AcOH mixture. The reaction was complete in 10 minutes. After 200 mL distilled water was added to the reaction mixture, the mixture was extracted with EtOAc. The organic layer was washed a few times with water and saturated sodium bicarbonate. The organic layer was then washed with brine solution and dried over sodium sulfate. Evaporation of the solvent provided the product as a yellow solid (10 g, yield=80%). LCMS (API-ES) m/z (%) 293.2 (100%, M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514566B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-bd2260f1577f4078b208e18d5c4b4dff |
| Source note | uspto-grants-2009_04 |