HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiobenzamide → 5-Ethyl-2-phenyl-1,3-thiazole-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiobenzamide | HCID 683563 | — |
| Reactant | Ethyl 3-bromo-2-oxopentanoate | HCID 14740334 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Ethyl-2-phenyl-1,3-thiazole-4-carboxylic acid | HCID 13835309 | — |
Reaction Steps
Intermediate 2C was prepared as described above for the preparation of intermediate 2B from 4.61 g of thiobenzamide, 5.0 g of ethyl 3-bromo-2-oxo-pentanoate, and 14 mL of toluene. Solids were collected and washed with cold water after cooling of the NaOH solution. Heating these solids with citric acid as described followed by cooling and isolation of the resulting solids gave 3.74 g (72% yield) of intermediate 2C; 1H NMR (CDCl3, 300 MHz) δ7913-7.91 (m, 2H), 7.51-7.50 (m, 3H), 3.39 (q, 2H, J=7.8), 1.42 (t, 3H, J=7.8); low resolution MS (ES+)m/e 233.81 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498174B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-6d6aae3e4bf6446399b3a3eab075c8cb |
| Source note | uspto-grants-2002_12 |