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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730407Generated: October 25, 2026

Hydrochloric Acid → 3-{3'-[(Tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxypropionic acid

https://huagongshe.com/reaction/730407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 3-{3'-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxypropionateHCID 68850052—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-{3'-[(Tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxypropionic acidHCID 68852083100.5%

Reaction Steps

0.65 g (1.3 mmol) of methyl 3-{3′-[(tert-butoxycarbonylmethylamino)-methyl]biphenyl-4-yl}-2-ethoxypropionate is placed in 10 ml of tetrahydrofuran, 0.5 ml of methanol and 1.9 ml (1.9 mmol) of aqueous 1M lithium hydroxide solution. After stirring at room temperature for 2 hours, the reaction medium is diluted with ethyl acetate, acidified to pH 6 with aqueous 1N hydrochloric acid solution, extracted with ethyl acetate, dried over magnesium sulfate, filtered and concentrated. 0.54 g of 3-{3′-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxypropionic acid is obtained in a yield of 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582663B2
Source datasetuspto-grants-2009_09
ORD IDord-5fec42d549c44d49abdc3ddecff830c8
Source noteuspto-grants-2009_09