HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 53884514, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | HCID 53420858 | HCID 53420858 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53884514 | HCID 53884514 | — |
Reaction Steps
To a solution of 1.75 g (10 mmol) of the above 4-(cyanomethyl) methyl benzoate (6) in 10 mL of EtOH was added 1.14 g (10 mmol) of cysteamine hydrochloride and 1.4 mL (10 mmol) of triethylamine. The reaction mixture was refluxed for 24 h. and evaporated to dryness. The residue was dissolved in CH2Cl2 (50 mL), washed with water and dried over Na2SO4. Removal of the solvent gave crude 7, which was crystallized from EtOH. Yield 2.1 g (89%); mp 67°-68° C.; NMR (CDCl3), δ8.0 (m, 2H, aromatic), 7.4 (m, 2H, aromatic), 4.2 (t, 2H, CH2), 3.9 (s, 3H CH3), 3.85 (s, 2H, CH2); IR (Nujol), 720 (ester), 1620 (C=N) cm-1 ; MS (EI) calculated for (C12H13NO2S), 235.00; found, 235 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05145854 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-c4c088f2f3774082b936ee9f2335eff9 |
| Source note | uspto-grants-1992_09 |