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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909128Generated: October 30, 2026

Tetraethylammonium tetrahydroborate → Methyl 2-(2-hydroxypropan-2-yl)-6-(4-methylphenyl)pyridine-4-carboxylate

https://huagongshe.com/reaction/1909128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethylammonium tetrahydroborateHCID 28251—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 2-(4-methylphenyl)-6-(prop-1-en-2-yl)pyridine-4-carboxylateHCID 67339741—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 2-(2-hydroxypropan-2-yl)-6-(4-methylphenyl)pyridine-4-carboxylateHCID 67339432—

Reaction Steps

To a solution of methyl 2-(4-methylphenyl)-6-(prop-1-en-2-yl)pyridine-4-carboxylate (191 mg, 0.71 mmol) in methanol (3.6 mL) and DME (3.6 mL) was added cobalt(II)mesotetraphenylporphine (2.4 mg, 3.6 mop. After 30 min, tetraethylammonium borohydride (170 mg, 1.17 mmol) was added in 3 portions over 1 h. Saturated aqueous NaHCO3 was added. The mixture was diluted with water and extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by reverse phase chromatography (C-18, 90% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (165 mg). MS 286.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598209B2
Source datasetuspto-grants-2013_12
ORD IDord-3240b01d78964a7f9c81768f8054afd4
Source noteuspto-grants-2013_12