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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175307Generated: November 1, 2026

Dimethylformamide → HCID 59557717, compound

https://huagongshe.com/reaction/1175307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 59557724HCID 59557724—
CatalystCupric ChlorideHCID 24014—
CatalystPalladium ChlorideHCID 24290—
ProductHCID 59557717HCID 5955771758.2%

Reaction Steps

A mixture of palladium chloride (159 mg, 0.053 mmol) and copper chloride (267 mg, 0.27 mmol) in DMF (3 mL) was stirred for 2.5 h at room temperature. (2S,3S,4R,5R,6R)-2-(2-(allyloxymethyl)-4-chloro-5-(4-ethylbenzyl)phenyl)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)tetrahydro-2H-pyran (intermediate O-1) (300 mg, 0.36 mmol) was added to the mixture and stirred overnight under oxygen. The reaction mixture was filtered, the filtrate was poured into water and extracted with ethyl acetate (20 mL×3). The combined extracts were dried over Na2SO4, filtered, and evaporated to dryness. The residue was purified by preparative TLC, which afforded 1-(5-chloro-4-(4-ethylbenzyl)-2-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)tetrahydro-2H-pyran-2-yl)benzyloxy)propan-2-one (intermediate T-1) (178 mg, 0.33 mmol, yield 58.2%). 1H-NMR (DMSO-d6, 300 MHz) δ 1.062 (t, J=8.1 Hz, 3H), 1.988 (s, 3H), 2.452 (dd, J=8.1 Hz, 2H), 3.603 (m, 6H), 3.793 (m, 2H), 3.997 (s, 2H), 4.125 (s, 2H), 4.491 (11, 7H), 4.744 (m, 4H), 6.789 (m, 2H), 7.015 (m, 4H), 7.169 (m, 5H), 7.288 (m, 13H), 7.457 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838498B2
Source datasetuspto-grants-2010_11
ORD IDord-97dc8a4204054af4871ea7d3f034d8e8
Source noteuspto-grants-2010_11