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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207579Generated: October 31, 2026

2-tert-Butyldimethylsilyloxymethyl-6-(1-methoxy-1-methylethyl)pyridine → 2-Hydroxymethyl-6-(1-methoxy-1-methylethyl)pyridine

https://huagongshe.com/reaction/2207579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyldimethylsilyloxymethyl-6-(1-methoxy-1-methylethyl)pyridineHCID 66718423—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Hydroxymethyl-6-(1-methoxy-1-methylethyl)pyridineHCID 66718434100.1%

Reaction Steps

A solution of 2-tert-butyldimethylsilyloxymethyl-6-(1-methoxy-1-methylethyl)pyridine (1.20 g, 4.08 mmol) in AcOH (45 mL), THF (15 mL) and H2O (15 mL) was stirred for 48 h at room temperature. The solvent was removed in vacuo, the residue was partitioned between DCM and sat aq NaHCO3, the organic portion was separated, dried (MgSO4), filtered and evaporated to give the title compound (740 mg, 100%) as a colourless oil; NMR δH (400 MHz, CDCl3) 7.70-7.66 (1H, m), 7.48-7.45 (1H, m), 7.07-7.04 (1H, m), 4.74 (2H, d, J 5.0 Hz), 4.14 (1H, t, J 5.0 Hz), 3.18 (3H, s), 1.57 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376443B2
Source datasetuspto-grants-2016_06
ORD IDord-ddb500e5aae1454180118e64ae36c64d
Source noteuspto-grants-2016_06