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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892195Generated: October 30, 2026

3-Hydroxybenzaldehyde → HCID 22241324, compound

https://huagongshe.com/reaction/892195

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantSodium hydrideHCID 24758—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 22241324HCID 22241324—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled suspension (0° C.) of 60% NaH (660 mg, 16.5 mmol) in THF (35 mL) is added dropwise a solution of 3-hydroxybenzaldehyde (1.89 g, 15 mmol) in THF (15 mL) and the resulting mixture stirred for 20 min. To the mixture is added 2-methoxyethoxymethyl chloride (1.88 mL, 16.5 mmol) and DMPU (5 mL), the cold bath removed and stirred for 1 hr. The reaction mixture is cooled to 0° C. then slowly added 2M NaBH4 (in triglyme) (3.75 mL, 7.5 mmol) and let stir for 1 hr. Slowly quenched with 2N HCl soln (3.9 mL) and diluted reaction mixture with ether. The organic layer is washed with brine, dried over MgSO4 and concentrated. The residue is purified by flash chromatography (silica, 60% ethyl acetate in hexanes) to give the title compound as a pale yellow oil. MS (EI) 212 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005440B1
Source datasetuspto-grants-2006_02
ORD IDord-8db9fa62e91c44639ce1682153cf6295
Source noteuspto-grants-2006_02