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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358898Generated: November 1, 2026

Water → 1-t-Butoxycarbonyl-3-dibenzylamino-4-methoxypyrrolidine

https://huagongshe.com/reaction/358898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-t-Butoxycarbonyl-3-dibenzylamino-4-hydroxypyrrolidineHCID 20067149—
SolventTetrahydrofuranHCID 8028—
Product1-t-Butoxycarbonyl-3-dibenzylamino-4-methoxypyrrolidineHCID 2006715480.5%

Reaction Steps

0.19 g (0.0047 mole) of sodium hydride (as a 60% w/w dispersion in mineral oil) and 0.89 g (0.0063 mole) of methyl iodide were added, in that order, to a solution of 1.2 g (0.0031 mole) of 1-t-butoxycarbonyl-3-dibenzylamino-4-hydroxypyrrolidine [prepared as described in Step (1) above] dissolved in 10 ml of tetrahydrofuran. The mixture was then stirred at room temperature for 5 hours. At the end of this time, water was added to the reaction mixture, which was then extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried and concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through silica gel, eluted with a 5:95 by volume mixture of ethyl acetate and toluene, to give 0.99 g of 1-t-butoxycarbonyl-3-dibenzylamino-4-methoxypyrrolidine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997943
Source datasetuspto-grants-1991_03
ORD IDord-04f769001bab4f64ade66d45a0e6d28c
Source noteuspto-grants-1991_03