Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant(7RS)-4-benzyl-7-(3,4-dichlorophenyl)-7-[(4-methoxyphenoxy)methyl]-1,4-oxazepan-3-oneHCID 66976203—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(7RS)-4-benzyl-7-(3,4-dichlorophenyl)-7-[(4-methoxyphenoxy)methyl]-1,4-oxazepaneHCID 6697579393.4%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-3a359658af204e4986acba26b38700fb
Source noteuspto-grants-2014_05