Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910593Generated: October 26, 2026

7-Chloro-2,3-dihydrobenzo[b][1,4]dioxine-5-carbaldehyde → 1-(6-Chloro-2,3-dihydrobenzo[b][1,4]dioxin-8-yl)ethanol

https://huagongshe.com/reaction/1910593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-2,3-dihydrobenzo[b][1,4]dioxine-5-carbaldehydeHCID 17944674—
ReactantHCID 178418689HCID 178418689—
SolventDiethyl EtherHCID 3283—
Product1-(6-Chloro-2,3-dihydrobenzo[b][1,4]dioxin-8-yl)ethanolHCID 58707260—

Reaction Conditions

Temperature0 °C

Reaction Steps

7-Chloro-2,3-dihydrobenzo[b][1,4]dioxine-5-carbaldehyde (0.26 g, 1.32 mmol) was dissolved in 10 mL of diethyl ether and cooled to 0° C. MeMgBr (1.1 mL, 3.31 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 (20 mL×2). The organic layer was dried over Na2SO4 and the solvent was removed by rotary evaporation to collect the desired product (258 mg, 91%). 1H NMR (400 MHz, CDCl3): δ 6.91 (s, 1H), 6.77 (s, 1H), 5.02 (m, 1H), 4.24 (m, 4H), 1.45 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604021B2
Source datasetuspto-grants-2013_12
ORD IDord-682025e16462419abc6dcf4ff6c4fce9
Source noteuspto-grants-2013_12