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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823644Generated: November 1, 2026

Salicyl Alcohol → o-Butoxybenzyl alcohol

https://huagongshe.com/reaction/1823644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicyl AlcoholHCID 5146—
ReactantButyl iodideHCID 10962—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
Producto-Butoxybenzyl alcoholHCID 2301450.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

2-Hydroxymethyl phenol (1.2 g, 9.6 mmol) was dissolved in 10 mL of dry acetonitrile. Potassium carbonate (1.3 g, 9.6 mmol) and 1-iodobutane (1 mL, 8.8 mmol) were added and the reaction was stirred at room temperature for 3 days and at 50° C. for 1 day. The solvent was removed and the residue partitioned between ethyl acetate and 1N hydrochloric acid. The acidic aqueous layer was extracted with ethyl acetate(3×25 mL). The combined organic extracts were washed with 0.5 N sodium hydroxide (3×20 mL), dried over MgSO4, filtered and concentrated to provide the title compound (800 mg, 50% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07038077B2
Source datasetuspto-grants-2006_05
ORD IDord-83402499895149f7be7343f8c6e3b96d
Source noteuspto-grants-2006_05