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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222670Generated: October 25, 2026

Sodium Carbonate → 7-(benzyloxy)-3-cyclobutyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

https://huagongshe.com/reaction/222670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantCyclobutanoneHCID 14496—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant7-(benzyloxy)-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 57437617—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product7-(benzyloxy)-3-cyclobutyl-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 10244716—

Reaction Steps

7-Benzyloxy-1,2,4,5-tetrahydro-benzo[d]azepine (D2) (25.3 g, 100 mmol) was dissolved in 2.5% acetic acid in dichloromethane (400 ml) at 0° C. and treated dropwise with cyclobutanone (11.2 ml, 150 mmol). The mixture was stirred for 30 minutes and then sodium triacetoxyborohydride (31.8 g, 150 mmol) was added portion wise. The reaction mixture was stirred at room temperature for 4 hours, basified with saturated sodium carbonate solution and extracted with dichloromethane. The combined extracts were washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The crude residue was triturated with hexane and filtered to afford the title product (E1). MS (ES+) m/e 308 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207331B2
Source datasetuspto-grants-2012_06
ORD IDord-7383a70fb69a46e9b3926021872b3989
Source noteuspto-grants-2012_06