HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-chlorosuccinamide → HCID 86669542, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-chlorosuccinamide | HCID 15238416 | — |
| Reactant | 76687-08-6 | HCID 83668651 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86669542 | HCID 86669542 | 86.2% |
Reaction Steps
2-(2-Amino-thiazol-4-yl)-2-methyl-propionic acid ethyl ester (0.3 g, 1.40 mmol) was taken in 10 mL of acetonitrile and N-Chlorosuccinamide (0.224 g, 1.68 mmol) was added the reaction was stirred for 1 hr. at room temperature. After completion of reaction acetonitrile was evaporated under reduced pressure and the residue was partitioned between water (25 mL) and ethyl acetate (25 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (2×25 mL). The combined organic layer was washed with brine and dried over anhydrous sodium sulphate and the solvent was removed in vacuo. The residue was purified by preparative TLC plate (mobile phase 40% ethyl acetate in hexane) to afford pure compound (0.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340506B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-718b0b7b56904ee99f0657950fe86525 |
| Source note | uspto-grants-2016_05 |