HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methyl-5-(2-hydroxyethyl)thiazole → 5-(2-Methanesulfonyl-ethyl)-4-methyl-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methyl-5-(2-hydroxyethyl)thiazole | HCID 1136 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(2-Methanesulfonyl-ethyl)-4-methyl-thiazole | HCID 18455442 | — |
Reaction Steps
Methanesulfonyl chloride (5.4 mmol) was added to a methylene chloride (0.2 M) solution of 5-(2-hydroxyethyl)-4-methyl-thiazole (4.5 mmol) and triethylamine (23 mmol), and stirred at room temperature overnight. The mixture was poured into water and extracted with methylene chloride. The organic extracts were washed with NaHCO3 (sat), and the product was extracted with 1M aq. HCl. The aqueous extracts were neutralized with NaHCO3 (sat) and then extracted with methylene chloride. The organic extracts were dried (MgSO4) and filtered. Solvent removal afforded product (5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939657B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-e8fd9f9401be4844a28d7005d786b9b4 |
| Source note | uspto-grants-2011_05 |