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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754289Generated: November 2, 2026

Benzyl Alcohol → Tert-butyl 5-benzyloxy-3-oxo-azepane-1-carboxylate

https://huagongshe.com/reaction/1754289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactanttert-Butyl 3-oxo-2,3,6,7-tetrahydro-1H-azepine-1-carboxylateHCID 75464896—
CatalystPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductTert-butyl 5-benzyloxy-3-oxo-azepane-1-carboxylateHCID 118222054183.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a mixture of tert-butyl 6-oxo-3,7-dihydro-2H-azepine-1-carboxylate (540.00 mg, 2.56 mmol, 1.00 Eq) in BnOH (2.76 g, 25.56 mmol, 10.00 Eq), was added t-BuOK (28.68 mg, 255.61 umol, 0.10 Eq) in one portion under N2. The mixture was stirred at 20° C. for 12 hours. LCMS showed the reaction was completed. The mixture was poured into water (100 mL) and stirred for 20 min. The aqueous phase was extracted with EA (40 mL*2). The combined organic phase was washed with saturated brine (20 mL*3), dried with anhydrous Na2SO4, filtered and concentrated in vacuum to afford tert-butyl 5-benzyloxy-3-oxo-azepane-1-carboxylate (1.50 g, crude) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169212B2
Source datasetuspto-grants-2015_10
ORD IDord-9032d3b27c114f96b9fa49931ccbcb07
Source noteuspto-grants-2015_10