Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176985Generated: October 30, 2026

Ethyl Acetate → 1-(1,3-Dioxaindan-5-yl)ethan-1-ol

https://huagongshe.com/reaction/2176985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAcetopiperoneHCID 76622—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-(1,3-Dioxaindan-5-yl)ethan-1-olHCID 22188286.3%

Reaction Steps

To a solution of 1-benzo[1,3]dioxol-5-yl-ethanone (2.5 gm; 15.2 mmol) in methanol (50 mL) is added sodium borohydride (634 mg; 16.7 mmol) in portions allowing for gas evolution. The reaction is stirred at room temperature for 3 hours before additional sodium borohydride is added to give a complete reaction by TLC (20% EA/Hex). The reaction is quenched with saturated ammonium chloride and extracted with ethyl acetate. The organics are separated, washed with water, dried over magnesium sulfate, and the solvent is removed to give 2.18 grams of 1-benzo[1,3]dioxol-5-yl-ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067897B2
Source datasetuspto-grants-2015_06
ORD IDord-0ce74a4ff9aa416ab0e902f10e103684
Source noteuspto-grants-2015_06