HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287630Generated: October 29, 2026
Chloromethyl Methyl Ether → HCID 21402946, compound
https://huagongshe.com/reaction/1287630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Dibenzosuberone | HCID 14589 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21402946 | HCID 21402946 | — |
Reaction Steps
A solution of chloromethyl methyl ether (40.2 g, 0.5 mole, freshly distilled) in dry tetrahydrofuran (80 ml) is prepared, and about 5 ml of that solution are added to a stirred mixture of magnesium turnings (12.0 g, 0.5 g - atom) and mercuric chloride (500 mg) in tetrahydrofuran (20 ml) until an exothermic reaction ensues. The flask is cooled to 0°± 10° and the remainder of the chloromethyl methyl ether solution is added dropwise with thorough agitation. After completion of addition a solution of 10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one (56.1 g 0.25 mole) in tetrahydrofuran is added dropwise. The reaction mixture is stirred overnight at room temperature and the complex is hydrolyzed with ice-cold ammonium chloride solution. The aqueous layer is extracted with ether (3 × 100 ml) and the combined extracts are washed with sodium chloride solution, dried and evaporated under reduced pressure to give 10,11-dihydro-5-methoxymethyl-5H-dibenzo[a,d]cyclohepten-5-ol as an oil with b.p. 143°- 144° C/0.05 mm, γmaxfilm : 3500 cm-1, 2820 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03985751 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-9c87685ce7b44373ad07ea923299251c |
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| Source note | uspto-grants-1976_10 |
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