HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3-chloropropyl)-4-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 3-Chloropropylamine | HCID 84629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-chloropropyl)-4-nitrobenzamide | HCID 3421653 | — |
Reaction Steps
A solution of 6.43 g (49 mmol) 3-chloropropylamine and 13.6 ml (98 mmol) triethylamine in 220 ml methylene chloride was cooled by an ice bath and 9 g (48.5 mmol) 4-nitrobenzoyl chloride were added fractionwise. After one hour stirring at room temperature the organic phase was washed twice with water, dried over MgSO4 and concentrated in vacuo to afford 10.68 g (91%). of beige crystals. 1H NMR was consistent with the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977179 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-f96156a5394c4311839ffe582a66b357 |
| Source note | uspto-grants-1999_11 |