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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473528Generated: October 30, 2026

HCID 131727738, compound → HCID 131727737, compound

https://huagongshe.com/reaction/473528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131727738HCID 131727738—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131727737HCID 13172773736%

Reaction Steps

10% Cd/Pb couple (455 mg, 3.71 mmol, 26 eq) was added to a rapidly stirring mixture of 17 (190 mg, 0.14 mmol), THF (3.2 mL) and 1 N NH4OAc (3.2 mL). The reaction mixture was allowed to stir for 6.5 hours when TLC showed the incomplete consumption of the starting material and formation of side products. The solids were filtered and rinsed with H2O and MeOH. Excess solvent was removed and the residue was diluted with H2O (25 mL) and DCM (25 mL). The aqueous layer was extracted with DCM (3×25 mL) and the organic extracts were combined, washed with brine (50 mL) and dried (MgSO4). Filtration and evaporation of solvent afforded the crude product which was purified by flash column chromatography (99:1 v/v CHCl3/MeOH then gradient to 98:2 v/v CHCl3/MeOH) to afford 18 as a yellow glass (38 mg, 36%): 1H NMR (400 MHz, CDCl3) δ 7.85 (d, 2H, J=3.9 Hz, H11), 7.77-7.65 (m, 6H, Harom), 7.59-7.50 (m, 6H, H3 and Harom), 7.47 (s, 2H, H6), 7.44-7.33 (m, 4H, Harom), 6.82 (s, 2H, H9), 4.42-4.32 (m, 2H, H11a), 4.31-4.14 (m, 4H, OCH2CH2CH2O), 3.89 (s, 6H, OCH3×2), 3.69-3.56 (m, 2H, H1), 3.50-3.37 (m, 2H, H1), 2.45-2.29 (m, 2H, OCH2CH2CH2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633185B2
Source datasetuspto-grants-2014_01
ORD IDord-e30c18fd351b4a0c8388fc1a1700cfb6
Source noteuspto-grants-2014_01