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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168052Generated: October 28, 2026

(S)-4-benzyloxy-2-(2-benzyloxyethoxy)-1-trityloxybutane → (S)-3-(2-hydroxyethoxy)-4-trityloxybutanol

https://huagongshe.com/reaction/1168052

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-4-benzyloxy-2-(2-benzyloxyethoxy)-1-trityloxybutaneHCID 10907940—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(S)-3-(2-hydroxyethoxy)-4-trityloxybutanolHCID 1078670778%

Reaction Conditions

Temperature50 °C

Reaction Steps

(S)-4-Benzyloxy-2-(2-benzyloxyethoxy)-1-trityloxy-butane (51 mg, 0.092 mmol) was dissolved in ethyl acetate (3 ml). To the solution was added 5% Pd—C (5.0 mg) and the mixture was stirred under an atmosphere of hydrogen for 15 hours at 50° C. After filtering off catalyst, the filtrate was condensed in vacuo, and the residue was subjected to silica gel chromatography to give (S)-3-(2-hydoxyethoxy)-4-trityloxybutanol (28 mg, yield 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620977B1
Source datasetuspto-grants-2003_09
ORD IDord-6170360ff1ff439fac79fe170033e79e
Source noteuspto-grants-2003_09