Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62769Generated: October 27, 2026

23138-53-6 → Methyl 4-(4-chloro-3-isopropoxy-5-methoxybenzamido)benzoate

https://huagongshe.com/reaction/62769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant23138-53-6HCID 280454—
ReactantHCID 67041857HCID 67041857—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(4-chloro-3-isopropoxy-5-methoxybenzamido)benzoateHCID 670415706.4%

Reaction Steps

n-Butyllithium (364 μl, 0.909 mmol) was slowly added to a solution of 2-chloro-5-iodo-1-isopropoxy-3-methoxybenzene (3) (270 mg, 0.827 mmol) in anhydrous THF (5 mL) at −78° C. After stirring for 15 min at this temperature a solution of methyl 4-isocyanatobenzoate (176 mg, 0.992 mmol) in anhydrous THF (5 mL) was added dropwise. The solution was allowed to warm to RT and stirred for a further 20 h. The reaction mixture was partitioned between DCM (40 mL) and brine (100 mL). The phases were separated and the organic solution was dried over MgSO4, filtered and the solvent was removed in vacuo. The residue was purified by silica gel chromatography (40 g, 0-40% EtOAc in isohexane) to afford methyl 4-(4-chloro-3-isopropoxy-5-methoxybenzamido)benzoate (5) (20 mg, 6%) as a colourless oil: m/z 376 [M−H]− (ES−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447028B2
Source datasetuspto-grants-2016_09
ORD IDord-b5154fa4399c4b45b1e11a47d77516ed
Source noteuspto-grants-2016_09