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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639032Generated: November 1, 2026

Methyl iodide → 5-Methyl-2,3-dihydrobenzo[B][1,4]dioxine-6-carbaldehyde

https://huagongshe.com/reaction/639032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
Reactant2,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 248127—
ReactantButyllithiumHCID 178418339—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
Product5-Methyl-2,3-dihydrobenzo[B][1,4]dioxine-6-carbaldehydeHCID 15767557—

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a solution of N,N,N′-trimethylethylenediamine (3.3 g, 32.3 mmol) in THF (100 mL) at −15° C. was dropwise added n-BuLi (19.2 mL, 30.5 mmol, 1.6 M in THF). After stirring at −15° C. for 15 minutes, a solution of solution of 1,4-benzodioxane-6-aldehyde (5.0 g, 30.5 mmol) in THF (10 mL). After 20 minutes, another batch of n-BuLi (5 mL, 3.1 mmol, 1.6 M in THF) was added and stirred for 3 h. The resulting solution was cooled down to −72° C. and the mixture was treated with MeI (25.9 g, 182.5 mmol) slowly. After stirring at −72° C. for 3 h, the mixture was diluted with HCl solution (1M in water). The aqueous layer was extracted several times with diethyl ether. The organic fractions were combined, concentrated and purified with column chromatography (silica, 5-40% ethyl acetate in hexane) to provide the title compound as an off-white compound (1.0 g, 18%): %): MS (ES) m/z 179 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691850B2
Source datasetuspto-grants-2010_04
ORD IDord-85b69fa64c8744358f10db513be707d2
Source noteuspto-grants-2010_04