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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070392Generated: October 25, 2026

Ammonium Chloride → Methyl 2-amino-5-phenylbenzoate

https://huagongshe.com/reaction/1070392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 2-amino-5-bromobenzoateHCID 736224—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 2-amino-5-phenylbenzoateHCID 1676879773.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of methyl 2-amino-5-bromobenzoate (2.0 g, 8.7 mmol) in dioxane (40 mL) were added phenylboronic acid (1.91 g, 15.7 mmol), potassium phosphate (4.08 g, 19.1 mmol) and tetrakis(triphenylphosphine)palladium (0.26 g, 0.22 mmol) under nitrogen. The mixture was heated at 85° C. for 20 h, then cooled to 0-5° C. Aqueous ammonium chloride was added and the mixture was extracted, washed with brine, dried (Na2SO4) and concentrated to dryness. Purification by chromatography gave 1.45 g of methyl 2-amino-5-phenylbenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903086B2
Source datasetuspto-grants-2005_06
ORD IDord-413eecf01edc47db99f6d12b91ff891e
Source noteuspto-grants-2005_06