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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292674Generated: October 30, 2026

1-Naphthaldehyde → N-[2(S)-(t-Butoxycarbonylamino)-3(S)-methylpentyl]-N-(1-naphthylmethyl)glycine methyl ester

https://huagongshe.com/reaction/1292674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(2(S)-(t-butoxycarbonylamino)-3(S)-methylpentyl)glycine methyl esterHCID 10755806—
Solvent1,2-DichloroethaneHCID 11—
ProductN-[2(S)-(t-Butoxycarbonylamino)-3(S)-methylpentyl]-N-(1-naphthylmethyl)glycine methyl esterHCID 10526565—

Reaction Steps

N-[2 (S)-(t-Butoxycarbonylamino)-3 (S)-methylpentyl] glycine methyl ester (2.00 g, 6.97 mmol) was dissolved in 1,2dichloroethane (56 ml) and 3A molecular sieves were added followed by 1-naphthaldehyde (1.89 ml, 13.9 mmol) and sodium triacetoxyborohydride (6.65 g, 31.4 mmol). The mixture was stirred at ambient temperature for 16 h, filtered and evaporated in vacuo. The residue was partitioned between EtOAc (100 ml) and sat. aq. NaHCO3 (25 ml). The aqueous layer was extracted with EtOAc (3×50 ml). The organic extracts were combined, dried (Na2 SO4), filtered, and evaporated in vacuo to afford a residue which was purified by chromatography (SiO2, 15-33% ethyl acetate in hexanes) to afford the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05756528
Source datasetuspto-grants-1998_05
ORD IDord-3b957b0633a546d99ee25796ebf0b8d9
Source noteuspto-grants-1998_05