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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426056Generated: November 2, 2026

6-Chlorobenzo[d][1,3]dioxole-4-carbaldehyde → 1-(5-Chlorobenzo[d][1,3]dioxol-7-yl)ethanol

https://huagongshe.com/reaction/2426056

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chlorobenzo[d][1,3]dioxole-4-carbaldehydeHCID 58707311—
ReactantHCID 178418689HCID 178418689—
SolventDiethyl EtherHCID 3283—
Product1-(5-Chlorobenzo[d][1,3]dioxol-7-yl)ethanolHCID 58707314—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Chlorobenzo[d][1,3]dioxole-4-carbaldehyde (147.0 mg, 0.79 mmol) was dissolved in 6 mL of diethyl ether and cooled to 0° C. MeMgBr (0.60 mL, 1.99 mmol) was added to the solution and the ice bath was removed. The reaction was allowed to stir at rt for 10 min. and at reflux for 30 min. The reaction was cooled to 0° C. and 10 mL of sat NH4Cl were added to quench the reaction. The diethyl ether layer was separated and washed with water (10 mL×2). The organic layer was dried over Na2SO4 and the solvent was removed by rotary evaporation to collect the desired product (155.0 mg, 98%). 1H NMR (400 MHz, CDCl3): δ 6.90 (d, 1H), 6.75 (d, 1H), 6.01 (d, 2H), 4.96 (m, 1H), 1.50 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968538B2
Source datasetuspto-grants-2011_06
ORD IDord-4423612db6774ff794c0600a5a8d7a27
Source noteuspto-grants-2011_06