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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62747Generated: October 29, 2026

Propylphosphonic anhydride → Methyl 4-(3-chloro-5-isopropoxy-4-methoxybenzamido)-2-methylbenzoate

https://huagongshe.com/reaction/62747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantHCID 67041734HCID 67041734—
Reactant3-Chloro-5-isopropoxy-4-methoxybenzoic acidHCID 67041762—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-(3-chloro-5-isopropoxy-4-methoxybenzamido)-2-methylbenzoateHCID 6704195141.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 3-chloro-5-isopropoxy-4-methoxybenzoic acid (5) (250 mg, 1.02 mmol), methyl 4-amino-2-methylbenzoate (6) (177 mg, 1.07 mmol) and TEA (150 μL, 1.07 mmol) in EtOAc (2.5 mL) was treated with T3P (50% in EtOAc) (1.63 mL, 2.55 mmol) and the mixture was heated at 60° C. for 5 h. The mixture was diluted with DCM (5 mL) and washed with 1M HCl (5 mL) followed by satd. NaHCO3 solution (5 mL). The organic solvents were removed in vacuo and the residue purified by silica gel chromatography (12 g, 0-100% EtOAc in isohexane to yield methyl 4-(3-chloro-5-isopropoxy-4-methoxybenzamido)-2-methylbenzoate (7) (167 mg, 40%): m/z 392 [M+H]+ (ES+), 390 [M−H]− (ES−). 1H NMR (400 MHz, CDCl3) δ:7.98 (1H, d), 7.78 (1H, s), 7.59-7.50 (2H, m), 7.40 (2H, dd), 4.67 (1H, sep), 3.94 (3H, s), 3.89 (3H, s), 2.62 (3H, s), 1.40 (6H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447028B2
Source datasetuspto-grants-2016_09
ORD IDord-91d471fa7af5481aa6e1236715a8cbd7
Source noteuspto-grants-2016_09