HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417052Generated: October 26, 2026
Sulfuric Acid → [3-Benzo[1,3]dioxol-5-yl-5-(4-methoxy-benzyloxy)-phenyl]-cyclopropyl-methanone
https://huagongshe.com/reaction/417052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Benzo[1,3]dioxol-5-yl-5-(4-methoxy-benzyloxy)-benzonitrile | HCID 59496839 | — |
| Reactant | HCID 178478986 | HCID 178478986 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-Benzo[1,3]dioxol-5-yl-5-(4-methoxy-benzyloxy)-phenyl]-cyclopropyl-methanone | HCID 59496824 | 91% |
Reaction Steps
To a solution of 3-benzo[1,3]dioxol-5-yl-5-(4-methoxy-benzyloxy)-benzonitrile (250 mg) in anhydrous THF (3 mL) were added a solution of cyclopropylmagnesium chloride (4.1 mL of 0.5 M solution in THF) and catalytic amount of cuprous bromide (2 mg). The resulting reaction mixture was refluxed for 1.5 h. After it was cooled down, 10% sulfuric acid (1.5 mL) was added and stirring was continued for 30 min at room temperature. Then the reaction mixture was diluted with diethyl ether, washed with water and brine. The organic extract was dried over anhydrous sodium sulfate, concentrated and purified on a silica gel column using ethyl acetate and hexanes to yield 253 mg of the title compound (91% yield). HRMS calcd for C25H22O5 [M+H]+ 403.1540, observed 403.1537.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088936B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-6af74d6d86da436ba62451dce57942bd |
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| Source note | uspto-grants-2012_01 |
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