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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376970Generated: October 30, 2026

Triethylamine → HCID 21099519, compound

https://huagongshe.com/reaction/2376970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 21099516HCID 21099516—
CatalystTitanium isopropoxideHCID 11026—
SolventEthanolHCID 702—
ProductHCID 21099519HCID 21099519—

Reaction Steps

A solution of 5-[(E)-2-(2,4-difluorophenyl)vinyl]-2-(phenylsulfonyl)benzaldehyde (prepared from Example 58 according to the method of Example 50 Step 1, 100 mg, 0.26 mmol), dimethylamine hydrochloride (50 mg, 0.62 mmol), titanium(IV) isopropoxide (0.2 mL, 0.62 mmol) and triethylamine (0.1 mL, 0.62 mmol) in ethanol (2 mL) was stirred at room temperature overnight. Sodium cyanoborohydride (35 mg, 0.56 mmol) was added and the reaction stirred for a further 3 hours. The solvent was removed in vacuo and the residue partitioned between water and ethyl acetate. The organic layer was washed with brine, dried over MgSO4 and evaporated in vacuo. The residue was purified by flash column chromatography on silica, eluting with 0-3% methanol/dichloromethane, to give the title compound as a white solid. δH (360 MHz, d6 DMSO): 8.12 (1H, d, J=8.2 Hz), 7.93-7.81 (5H, m), 7.68-7.56 (3H, m), 7.38 (2H, s), 7.33-7.27 (1H, m), 7.14 (1H, td, J=2.4, 8.5 Hz), 3.57 (2H, s), 1.88 (6H, s). m/z (ES+) 414 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468393B2
Source datasetuspto-grants-2008_12
ORD IDord-44ba2513c93c464f8f35ac9aeb326e2a
Source noteuspto-grants-2008_12