HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(5-Chloro-pentanoylamino)-5-nitro-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Chlorovaleryl chloride | HCID 74089 | — |
| Reactant | Methyl 3-amino-5-nitrobenzoate | HCID 2756518 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(5-Chloro-pentanoylamino)-5-nitro-benzoic acid methyl ester | HCID 69357073 | 124.6% |
Reaction Steps
5-Chlorovaleryl chloride (2.64 g, 17 mmol, 1.1 equiv) in CH2Cl2 (5 ml) was added over 2 min to a stirred solution of 3-amino-5-nitro-benzoic acid methyl ester (D1) (3 g, 15.3 mmol, 1 equiv) and NEt3 (2.6 ml, 18 mmol, 1.2 equiv) in CH2Cl2 (30 ml). The resulting mixture was stirred for 1 h at room temperature then washed with 2N aqueous HCl solution, dried over MgSO4 and concentrated in vacuo. The residue was triturated with CH2Cl2 to give 3-(5-Chloro-pentanoylamino)-5-nitro-benzoic acid methyl ester D3 (6 g, 112%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253198B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-9759496f4dff403ea5fab7ba35909980 |
| Source note | uspto-grants-2007_08 |