HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46472Generated: October 28, 2026
Hydrogen Peroxide → 2-Benzylidene-1-tetralone oxide
https://huagongshe.com/reaction/46472
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Benzylidene-3,4-dihydronaphthalen-1-one | HCID 111179 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Benzylidene-1-tetralone oxide | HCID 86736690 | 102.2% |
Reaction Steps
Ten grams (0.043 mole) of 2-benzylidene-1-tetralone (prepared as described in U.S. Pat. No. 3,926,988) is dissolved in 650 ml of MeOH at 35°, stirred, and treated with 10.5 g (0.092 mole) of 30% H2O2, followed by 10.5 ml (0.042 mole) of 16% NaOH solution while maintaining the temperature at 35°-36°. After stirring for 4 hours at room temperature, the solution is concentrated to approximately 50 ml on a rotary evaporator (high vacuum, low heat), diluted with 250 ml of cold H2O (an oil separates), extracted with ether (200 ml; then 4×100 ml), the combined ether layers dried (MgSO4), and the solvent evaporated to give 11.0 g (100%) of a semi-crystalline residue. Crystallization (of 10.6 g) from 55 ml of (i-Pr)2O gives 8.3 g (80%) of colorless solid; m.p. 71°-73°. Lit m.p. 77°-77.5° [JACS, 79, 232 (1957)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04173634 |
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| Source dataset | uspto-grants-1979_11 |
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| ORD ID | ord-36b2780cf9654c4293ba313dfa5cbe67 |
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| Source note | uspto-grants-1979_11 |
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