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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445448Generated: October 31, 2026

Water → 2-[2-(Tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoic acid

https://huagongshe.com/reaction/1445448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 2-[2-(tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoateHCID 68530686—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product2-[2-(Tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoic acidHCID 6853427391%

Reaction Steps

Methyl 2-[2-(tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoate (1.0 g, 3.07 mmol) was suspended in 20 ml of 3:1 tetrahydrofuran (THF):water, then chilled on ice for 30 min with stirring. Next there was added solid lithium hydroxide monohydrate (284 mg, 6.76 mmol) to the suspension, and the mixture was stirred at room temperature for 20 h at which time TLC (50:50:1 hexanes:EtOAc:AcOH) showed complete consumption of starting ester. The slurry was diluted with water (50 ml), washed twice with ethyl ether, then the aqueous layer was acidified to pH 2 with 1 N NaHSO4 to yield a heavy white slurry. The slurry was extracted twice with EtOAc, then the EtOAc layers were combined, washed with brine, dried over Na2SO4, and concentrated in vacuo to provide 2-[2-(tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoic acid (870 mg, 91%) as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666866B2
Source datasetuspto-grants-2010_02
ORD IDord-293df42beaf144a8ae761a683e0d7f93
Source noteuspto-grants-2010_02