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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886884Generated: November 1, 2026

Benzyl 5-(bis(4-methoxyphenyl)(phenyl)methoxy)-3-hydroxypentylcarbamate → 1-Amino-5-(bis(4-methoxyphenyl)(phenyl)methoxy)pentan-3-ol

https://huagongshe.com/reaction/1886884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 5-(bis(4-methoxyphenyl)(phenyl)methoxy)-3-hydroxypentylcarbamateHCID 68749958—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-Amino-5-(bis(4-methoxyphenyl)(phenyl)methoxy)pentan-3-olHCID 68745474—

Reaction Steps

Benzyl 5-(bis(4-methoxyphenyl)(phenyl)methoxy)-3-hydroxypentylcarbamate (15.4 g, 27.7 mmoles) is dissolved in methanol (250 mL) and the solution is poured into a hydrogenation flask. 10% Palladium on carbon (1.5 g, 50% water by weight) is added, and the flask is sealed. The atmosphere in the flask is evacuated using a diaphragm pump, and replaced with dry argon to 10 psi. This cycle of evacuation/argon purging is repeated four more times. The flask is then evacuated once more and filled with hydrogen to 30 psi. The suspension is stirred briskly at ambient temperature for 16 hours. Hydrogen is replaced to 30 psi as necessary during the first four hours of reaction. The flask is then evacuated to remove hydrogen, and refilled with argon to atmospheric pressure. The catalyst is removed by filtration using a 0.45 μm nylon membrane, and washed with methanol (100 mL). The combined methanol filtrates are evaporated to dryness to give a white glassy foam, which is further dried in vacuo. The yield is 11.4 g (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501706B2
Source datasetuspto-grants-2013_08
ORD IDord-aae22cc1f22a41b98b7d4e64b67675b6
Source noteuspto-grants-2013_08