HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 11821667, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 22066151 | HCID 22066151 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 11821667 | HCID 11821667 | — |
Reaction Steps
400 mg (2.1 mmol) of N-bromosuccinimide was added into 10 ml of anhydrous chloroform with 400 mg (2.1 mmol) of 5-methoxy-2-phenylthiazole under 0° C. condition and was stirred for 4 hours at a room temperature. After completion of reaction, the organic phase was extracted with ethyl acetate, and was dried with addition of magnesium sulfate. After removing the solvent, the product was developed with ethyl acetate:hexane=1:3 solvent on silica column to give 4-bromo-5-methoxy-2-phenylthiazole (Rf=0.50). The yield was 550 mg in weight and 97% in percentage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07057054B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-d31fa127692248f28b9ebd3d66c10841 |
| Source note | uspto-grants-2006_06 |