HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022589Generated: October 31, 2026
Aluminum(III) Chloride → (7RS)-4-benzyl-7-(3,4-dichlorophenyl)-7-[(4-methoxyphenoxy)methyl]-1,4-oxazepane
https://huagongshe.com/reaction/1022589
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | (7RS)-4-benzyl-7-(3,4-dichlorophenyl)-7-[(4-methoxyphenoxy)methyl]-1,4-oxazepan-3-one | HCID 66976203 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (7RS)-4-benzyl-7-(3,4-dichlorophenyl)-7-[(4-methoxyphenoxy)methyl]-1,4-oxazepane | HCID 66975793 | 93.4% |
Reaction Steps
To a solution of lithium aluminum hydride (934 mg) in diethyl ether (30 mL) was added aluminum chloride (1.09 g), and the mixture was stirred at 0° C. for 10 min. To the reaction mixture was added dropwise a solution of (7RS)-4-benzyl-7-(3,4-dichlorophenyl)-7-[(4-methoxyphenoxy)methyl]-1,4-oxazepan-3-one (6.02 g) in THF (30 mL), and the mixture was stirred at 0° C. for 15 min, and stirred while warming to room temperature for 2 hr. To the reaction mixture was added ice, and the precipitate was filtered off through celite. The filtrate was diluted with water, and the mixture was extracted with ethyl acetate. The obtained extract was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (5.46 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722662B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-3a359658af204e4986acba26b38700fb |
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| Source note | uspto-grants-2014_05 |
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