HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-chloroacrylate → 5-Chloro-5-methoxycarbonyl-3-thiapentanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-chloroacrylate | HCID 6659 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Mercaptoacetamide | HCID 12961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-Chloro-5-methoxycarbonyl-3-thiapentanamide | HCID 19875485 | 85.8% |
Reaction Steps
2-Mercaptoacetamide (10.0 g) and methyl 2-chloroacrylate (13.24 g) were dissolved in warm acetone (100 ml), and potassium carbonate (7.58 g) was added in one portion. Heat was evolved. The mixture was heated to reflux for 2 hours. The red solution was filtered hot using a filter aid, and the residue washed with hot acetone (×2). The filtrate and washings were combined and evaporated to obtain the title compound as a red oil (19.92 g) 1H n.m.r. δ (CDCl3 /DMSO-d6) 3.05-3.18 (4H, overlapping s and d, CH2COR and CH2CH) 3.76 (3H,s,CO2Me), 4.67 (1H,t, J=7Hz, CHCH2), 6.92 (1H, br s, CONH), 7.43 (1H, br s, CONH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153330 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-5cd356e6551d41bd8ac6635d16a16d4c |
| Source note | uspto-grants-1992_10 |