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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012207Generated: October 31, 2026

1,2-Dimethoxyethane → HCID 86633103, compound

https://huagongshe.com/reaction/1012207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 72994854HCID 72994854—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
ProductHCID 86633103HCID 86633103368%

Reaction Steps

To a N2-purged flask was added ′5-[1-[4-(2,4-bis-trifluoromethyl-benzyloxy)-3-methoxy-phenyl]-methylidene]-2-thioxo-thiazolidin-4-one (42 mg, 85 μmol) and DME (4 mL). To the solution was added NaBH3CN (20 mg, 255 μmol) followed by acetic acid (2 mL). The reaction was stirred at rt for 2 h. The reaction solution was then diluted with EtOAc (100 mL), neutralized by successive washings of sat NaHCO3 (100 mL×3), washed with sat. NaCl (100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The crude material was chromatographed (SiO2, DCM/MeOH 100:0 to 98:2) to provide intermediate compound (155 mg, 50% yield). 1H NMR (CDCl3) δ 9.29 (1H, br s), 7.99 (1H, d, J=8.1 Hz), 7.94 (1H, s), 7.83 (1H, d, J=8.1 Hz), 6.72-6.81 (3H, m), 5.38 (2H, s), 4.60 (1H, dd, J1=3.9 Hz, J2=9.8 Hz), 3.92 (3H, s), 3.48 (1H, dd, J=3.9 Hz, J2=14.2 Hz), 3.14 (1H, m); MS (ESI) 496 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977489B2
Source datasetuspto-grants-2011_07
ORD IDord-4996c4ff91a74336a8a7700efd8f84dd
Source noteuspto-grants-2011_07