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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175314Generated: November 2, 2026

HCID 59557700, compound → HCID 25168848, compound

https://huagongshe.com/reaction/1175314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59557700HCID 59557700—
CatalystPalladiumHCID 23938—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 25168848HCID 2516884851%

Reaction Steps

A mixture of (2R,3R,4R,5S,6S)-3,4,5-tris(benzyloxy)-2-(benzyloxymethyl)-6-(4-chloro-5-(4-ethylbenzyl)-2-(2-(2,2,2-trifluoroethoxy)ethyl)phenyl)tetrahydro-2H-pyran (30 mg, 0.034 mmol) and 10% Pd/C (30 mg) in 6 mL of MeOH:THF (1:1) was stirred under H2 atmosphere (1 atm) for 2 h. The mixture was filtered, and the filtrate was concentrated to provide the crude product, which was purified by HPLC to yield 9 mg of title compound. 1H-NMR (CD3OD, 300 MHz) δ 7.40 (s, 1H), 7.27 (s, 1H), 7.10 (s, 4H), 4.44-4.41 (m, 1H), 4.06 (d, J=15.3 Hz, 1H), 4.00 (d, J=15.3 Hz, 1H), 3.95-3.79 (m, 5H), 3.67-3.61 (m, 1H), 3.48-3.46 (m, 2H), 3.39-3.36 (m, 2H), 3.15-3.05 (m, 1H), 2.98-2.91 (m, 1H), 2.58 (q, J=7.6 Hz, 2H), 1.19 (t, J=7.6 Hz, 3H); MS ESI (m/z) 519 (M+1)+, calc. 518.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838498B2
Source datasetuspto-grants-2010_11
ORD IDord-6627b689b7d04d27bdd01dc426f50c32
Source noteuspto-grants-2010_11