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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201778Generated: October 26, 2026

Ammonia → Dimethyl 2,6-dichloroterephthalate

https://huagongshe.com/reaction/2201778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSulfuric AcidHCID 1118—
ReactantPhosphinic AcidHCID 4124402—
ReactantDimethyl 2-amino-3,5-dichloroterephthalateHCID 20714731—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
ProductDimethyl 2,6-dichloroterephthalateHCID 773022779%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a round bottom flask containing concentrated sulfuric acid (10 mL) was added ice-cold water (10 mL) while maintaining the temperature around 0° C. Sodium nitrite (3.7 g, 53 mmol) was added portion wise followed by the drop wise addition of hypophosphorous acid (8 mL). This was followed by drop wise addition of a solution of dimethyl 2-amino-3,5-dichlorobenzene-1,4-dicarboxylate (5 g, 17.9 mmol, Step a) in acetic acid (10 mL). The resulting reaction mixture was stirred at 0° C. for 2 hours and then stored in a refrigerator at −10° C. for 15 hours. The reaction mixture was stirred at room temperature for additional 2 hours. The reaction mixture was again cooled to 0° C. and neutralized with aqueous ammonia solution, partitioned with ethyl acetate (2×15 mL). The combined organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by silica gel column chromatography using ethyl acetate in hexane (4%) to yield dimethyl 2,6-dichlorobenzene-1,4-dicarboxylate as a pale yellow crystalline solid (3.8 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364466B2
Source datasetuspto-grants-2016_06
ORD IDord-56d09ad16ee44e0fa5a1685abfc1703c
Source noteuspto-grants-2016_06