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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891625Generated: October 27, 2026

[2-(t-Butyldiphenylsilyloxy)ethyl]carbamic acid benzyl ester → 2-(t-Butyldiphenylsilyloxy)ethylamine

https://huagongshe.com/reaction/891625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(t-Butyldiphenylsilyloxy)ethyl]carbamic acid benzyl esterHCID 16221537—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product2-(t-Butyldiphenylsilyloxy)ethylamineHCID 1100104372.1%

Reaction Steps

A solution of [2-(t-butyldiphenylsilyloxy)ethyl]carbamic acid benzyl ester (3.01 g, 6.9 mmol) (obtained as described in Reference Example 33(1)) in methanol (150 ml) was subjected to catalytic hydrogenation in the presence of 20% palladium hydroxide on charcoal (3.0 g) at room temperature. After checking the completion of the reaction, the reaction mixture was filtered in order to remove the catalyst and the filtrate concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using methylene chloride:methanol (10:1) as the eluant to afford 2-(t-butyldiphenylsilyloxy)ethylamine (1.49 g, yield 72%) as a pale brown syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-8bcababc24424e45b23036004945c6c9
Source noteuspto-grants-2006_02