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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505648Generated: November 1, 2026

Sodium Hydroxide → 3-(Phenylmethyl)-7-oxa-3-azabicyclo[4.1.0]heptane

https://huagongshe.com/reaction/1505648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-bromobutanimideHCID 67184—
Reactant1-BENZYL-1,2,3,6-TETRAHYDROPYRIDINEHCID 6421573—
CatalystTrifluoroacetic acidHCID 6422—
SolventWaterHCID 962—
Product3-(Phenylmethyl)-7-oxa-3-azabicyclo[4.1.0]heptaneHCID 64214963,337.2%

Reaction Steps

3.36 g of 1-benzyl-1,2,3,6-tetrahydropyridine (0.19 mmol) was dissolved in 35 mL of water containing 1.5 mL of trifluoroacetic acid (0.2 mmol). To that solution 5.87 g of NBS was added in small portions. After 4 hs reaction mixture was transferred to 50 mL of 20% NaOH solution and stirred overnight. On the morning reaction mixture was extracted with dichloromethane and combined organic fractions were dried over sodium sulfate and concentrated. The residue was purified on silica gel column using hexane-ethyl acetate 3:1 as eluent. Evaporation of solvent produced 1.2 g of 3-benzyl-7-oxa-3-azabicyclo[4.1.0]heptane as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216993B2
Source datasetuspto-grants-2015_12
ORD IDord-079f2d5f617c48c29b82e2586a37ac3c
Source noteuspto-grants-2015_12