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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259967Generated: October 30, 2026

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

https://huagongshe.com/reaction/259967

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 1,2-dichloroethane (56 ml) and 3A molecular sieves were added followed by 1-naphthaldehyde (1.89 ml, 13.9 mmol) and sodium triacetoxyborohydride (665 g, 31.4 mmol). The mixture was stirred at ambient temperature for 16 h, and filtered through glass fiber paper and concentrated. The residue was partitioned between EtOAc and sat. NaHCO3 (100 ml/25 ml). The aqueous layer was extracted with EtOAc (3×50 ml). The organic layers were combined, dried (Na2SO4), filtered, and Concentrated to give 5.0 g of crude product which was purified by chromatography (SiO2, 15-33% ethyl acetate/hexane) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523456
Source datasetuspto-grants-1996_06
ORD IDord-39281dd44897474a9df24c3d16165f1a
Source noteuspto-grants-1996_06