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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432122Generated: November 2, 2026

Sodium Carbonate → HCID 68542335, compound

https://huagongshe.com/reaction/1432122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantThionyl ChlorideHCID 24386—
ReactantN-Ethylprop-2-en-1-amine--hydrogen chloride (1/1)HCID 20193693—
ReactantHCID 69357330HCID 69357330—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 68542335HCID 68542335—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 1.0 g (4.45 mmol) 5-ethoxy-isophthalic acid mono methyl ester, 10 ml toluene and 0.5 ml SOCl2 is treated with one drop DMF and heated to 80° C. till the evolution of gas ceases. After cooling down the mixture is evaporated, dissolved in 5 ml DCM and added to an at 0° C. stirred mixture of 10 ml 10% aqueous Na2CO3, 0.81 g (6.7 mmol) allyl ethyl amine hydrochloride (see IVb) and 5 ml DCM. After 1 h the layers are separated and the organic layer is washed with 1N HCl, brine, dried with sodium sulfate and evaporated to yield the N-allyl-5-ethoxy-N-ethyl-isophthalamic acid methyl ester. This ester is dissolved in 20 ml MeOH, treated with 15 ml 1N NaOH and stirred for 18 h. The methanol is evaporated, the residue acidified with 1N HCl and extracted with TBME. The organic layer is dried with sodium sulfate and evaporated to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612055B2
Source datasetuspto-grants-2009_11
ORD IDord-e7476d40055c46dc99ac3b0978a76023
Source noteuspto-grants-2009_11