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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417905Generated: November 3, 2026

Triethylamine → methyl N-(BOC)-8-aminomethyl-5,6,7,8-tetrahydro-2-naphthoate

https://huagongshe.com/reaction/1417905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantMethyl 8-(aminomethyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylateHCID 14756556—
SolventTetrahydrofuranHCID 8028—
Productmethyl N-(BOC)-8-aminomethyl-5,6,7,8-tetrahydro-2-naphthoateHCID 1935919347.2%

Reaction Steps

A solution of methyl 8-aminomethyl-5,6,7,8-tetrahydro-2-naphthoate (0.78 g, 0.0036 mol) and triethylamine (0.55 mL, 0.40 g, 0.004 mol) in aqueous tetrahydrofuran (50%, 75 mL) was added, portionwise as a solid, 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (0.99 g, 0.004 mol). All was stirred at ambient temperature over 3 hours. The solution was concentrated to half volume and extracted with diethylether. The aqueous layer was then acidified to a pH of 1.0 using hydrochloric acid (1N) and then extracted with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The residue was purified by flash chromatography using hexane:ethyl acetate::8:2 to give methyl N-(BOC)-8-aminomethyl-5,6,7,8-tetrahydro-2-naphthoate (0.54 g, 0.0017 mol, 47%) as a white solid. mp=72°-80° C.; 1H NMR (DMSO) d 13.8 (s, 1H), 7.8-7.65 (m, 3H), 7.6-7.5 (m, 3H), 7.25-7.20 (m, 1H), 7.15-7.05 (m, 1H), 3.9-3.8 (m, 1H), 3.2-2.8 (m, 4H), 1.8-1.6 (m, 3H), 1.4 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05879657
Source datasetuspto-grants-1999_03
ORD IDord-373dab26ee6f4d10b8c088fc3c6bcb03
Source noteuspto-grants-1999_03