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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446543Generated: October 30, 2026

Sodium Hydroxide → 4-[2-(N-Boc-N-methylamino)ethyl]benzoic acid

https://huagongshe.com/reaction/446543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-{2-[(tert-butoxycarbonyl)(methyl)amino]ethyl}benzoateHCID 58393325—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(N-Boc-N-methylamino)ethyl]benzoic acidHCID 6667136274%

Reaction Steps

The resulting methyl 4-{2-[(tert-butoxycarbonyl)(methyl)amino]ethyl}benzoate (200 mg, 0.682 mmol) was dissolved in tetrahydrofuran (4 mL), a 1 N aqueous sodium hydroxide solution (1 mL) was added under ice cooling, and the mixture was stirred at room temperature for 16 hours. After the reaction was completed, the aqueous layer was washed with ethyl acetate, the aqueous layer was adjusted to pH 3 with a 1 N aqueous hydrochloric acid solution, and then ethyl acetate was further added to separate the layers. The resulting organic layer was separated, washed with saturated sodium chloride solution, and then dried with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give a crude title compound (140 mg; yield, 74%) as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476253B2
Source datasetuspto-grants-2013_07
ORD IDord-eb5d4855452c4a95a99d5efcbe8f7035
Source noteuspto-grants-2013_07