HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520834Generated: October 30, 2026
Triethylamine → Methyl 5-bromo-2-(2-(4-cyanophenoxy)acetamido)benzoate
https://huagongshe.com/reaction/520834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 2-amino-5-bromobenzoate | HCID 736224 | — |
| Reactant | Acetyl chloride, (4-cyanophenoxy)- | HCID 12207748 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-bromo-2-(2-(4-cyanophenoxy)acetamido)benzoate | HCID 8112554 | — |
Reaction Steps
To a solution of methyl 2-amino-5-bromobenzoate (4.0 g, 17.39 mmol) in dichloromethane (60 mL) was added 2-(4-cyanophenoxy)acetyl chloride (3.74 g, 19.13 mmol, Intermediate 2: step a) to form a thick suspension. An additional 30 mL of dichloromethane was added. The reaction was then cooled to 0° C. and triethylamine (5.32 mL, 38.25 mmol) was added dropwise. The cold bath was removed and the reaction was stirred at room temperature for 2 hours, then filtered to give the title compound as a white solid. The filtrate was washed with water, followed by saturated aqueous NH4Cl solution. The organic layer was dried (MgSO4), filtered, concentrated, and the residue was purified by flash column chromatography (silica gel, 20% EtOAc-heptane) to afford more of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09328095B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-3a118594e5f545bab24dbba9266820d9 |
|---|
| Source note | uspto-grants-2016_05 |
|---|