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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269565Generated: November 2, 2026

Methanol → HCID 87829163, compound

https://huagongshe.com/reaction/1269565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 18448755HCID 18448755—
CatalystThionyl ChlorideHCID 24386—
ProductHCID 87829163HCID 87829163—

Reaction Steps

3,5-Dichloro-4-(4-amino-3-nitrophenoxy)phenylacetic acid (50 mg), methanol (20 mL) and thionyl chloride (2 drops) was heated at reflux for two hours. After cooling down to room temperature, the reaction mixture was partioned between an aqueous solution of sodium hydrogencarbonate (saturated) and ethyl acetate. The organic phase was washed with brine and concentrated. This gave 45 mg of methyl(3,5-dichloro-4-(4-amino-3-nitro-phenoxy)phenyl) acetate which was reduced using the method described in Example 1(f), to give 40 mg of methyl(3,5-dichloro-4-(3,4-diaminophenoxy)phenyl) acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199265B2
Source datasetuspto-grants-2007_04
ORD IDord-54b417ab2eeb47d39c1b658cf3e0763b
Source noteuspto-grants-2007_04