HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349434Generated: November 1, 2026
2-Methoxybenzaldehyde → HCID 22382435, compound
https://huagongshe.com/reaction/1349434
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxybenzaldehyde | HCID 8658 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178420628 | HCID 178420628 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22382435 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07211685B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-31fe12f89bdd4d58981baf700c5c4923 |
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| Source note | uspto-grants-2007_05 |
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