HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylglycine → HCID 54316039, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | 2-Thiophenecarboxaldehyde, 5-chloro- | HCID 81700 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 54316039 | HCID 54316039 | 100% |
Reaction Steps
A mixture consisting of 5-chlorothiophene-2-carboxaldehyde (1.00 g, 6.82 mmol), N-acetylglycine (0.96 g, 8.18 mmol), NaOAc (0.67 g, 8.18 mmol) in Ac2O (5 mL) is warmed at reflux for 16 hours. The reaction mixture is cooled to ambient temperature and diluted with dilute aqueous NaOH (0.5 M, 100 mL) and CH2Cl2 (100 mL). The layers are separated and the organic phase is washed with aqueous NaHCO3, brine, dried over anhydrous Na2SO4, filtered and concentrated to provide 1.5 g (100%) of the title compound as a colorless oil which is used without further purification in the next reaction. 1H NMR (300 MHz, CDCl3) δ2.39 (s, 3H), 6.94 (d, J=4.0 Hz, 1H), 7.21 (s, 1H), 7.26 (d, J=4.0 Hz, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612075B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-da6c9100ec0446b181cb1583437fc61e |
| Source note | uspto-grants-2009_11 |