HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → Methyl 4-(2-benzenecarbonylamino-ethoxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 4-(2-aminoethoxy)benzoate hydrochloride | HCID 50988568 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-(2-benzenecarbonylamino-ethoxy)benzoate | HCID 14426627 | — |
Reaction Steps
To a suspension of methyl 4-(2-amino-ethoxy)benzoate hydrochloride (0.232 g, 1 mmol) in THF (6 ml) was added benzoyl chloride (0.140 g, 1 mmol) followed by triethylamine (0.121 g, 1.2 mmol). The reaction mixture was stirred for 1 h and then diluted with ethyl acetate. The organic layer was washed with 0.5 M aqueous HCl, saturated sodium bicarbonate solution, and brine. The organic layer was concentrated in vacuo to give methyl 4-(2-benzenecarbonylamino-ethoxy)benzoate which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026371B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-063f758d88ab43dda9c772f97302fa97 |
| Source note | uspto-grants-2011_09 |