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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349434Generated: November 1, 2026

2-Methoxybenzaldehyde → HCID 22382435, compound

https://huagongshe.com/reaction/1349434

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxybenzaldehydeHCID 8658—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178420628HCID 178420628—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22382435HCID 22382435—

Reaction Steps

Magnesium (10.7 g) was suspended in tetrahydrofuran (80 ml), and to the suspension was added iodine (5 mg). Bromocyclopropane (32.0 ml) was added dropwise thereto over 1.5 hr and the mixture was heated under reflux for 1.5 hr. Thereto was added tetrahydrofuran to give a 1M cyclopropylmagnesium bromide-tetrahydrofuran solution. Subsequently, o-anisaldehyde (8.17 g) was dissolved in tetrahydrofuran (150 ml), the 1M cyclopropylmagnesium bromide-tetrahydrofuran solution (90 ml) was added dropwise thereto over 50 min under ice-cooling, and the mixture was stirred at room temperature for 12 hr. The reaction mixture was ice-cooled, a saturated aqueous ammonium chloride solution (9 ml) was added, and the reaction mixture was stirred at room temperature for 30 min. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=9:1) to give the title compound (6.13 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211685B2
Source datasetuspto-grants-2007_05
ORD IDord-31fe12f89bdd4d58981baf700c5c4923
Source noteuspto-grants-2007_05