HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627464Generated: October 30, 2026
Phenylacetyl chloride → Methyl 5-bromo-2-(2-phenylacetamido)benzoate
https://huagongshe.com/reaction/627464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-amino-5-bromobenzoate | HCID 736224 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-bromo-2-(2-phenylacetamido)benzoate | HCID 19168685 | — |
Reaction Steps
To a mixture of methyl 2-amino-5-bromobenzoate (9.00 g, 39.1 mmol) and Et3N (7.6 mL, 54.8 mmol) in CH2Cl2 (90 mL) was added 2-phenylacetyl chloride (7.26 g, 46.9 mmol) at 4° C. dropwise. After completion of the addition, the cooling bath was removed and the mixture was stirred for 27 hours. TLC showed some of the starting material methyl 2-amino-5-bromobenzoate still remained. More 2-phenylacetyl chloride (1.88 g, 12.2 mmol) and Et3N (2.2 mL, 15.9 mmol) were added, and the mixture was stirred overnight. K2CO3 (aqueous) was added, the organic layer was separated, and the aqueous layer was extracted with CH2Cl2. The combined organic layers were washed with water, dried (Na2SO4), filtered, and concentrated in vacuo. CH3CN (100 mL) was added, and the precipitated solid was filtered, washed with Et2O, and dried to give the title compound. The filtrate was concentrated in vacuo, and the solid was filtered, washed with Et2O, and dried to give more title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09309222B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-22bfb6df96e14543881847cd7113bd89 |
|---|
| Source note | uspto-grants-2016_04 |
|---|