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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975821Generated: October 31, 2026

Formaldehyde → 2-Acetyl-3,8-dimethyl-8-azabicyclo[3.2.1]oct-2-ene

https://huagongshe.com/reaction/1975821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-Acetyl-3-methyl-8-azabicyclo[3.2.1]oct-2-eneHCID 19751356—
SolventAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
Product2-Acetyl-3,8-dimethyl-8-azabicyclo[3.2.1]oct-2-eneHCID 19098820—

Reaction Steps

To a stirred mixture of 2-acetyl-3-methyl-8-azabicyclo [3.2.1]oct-2-ene (1,2083 g, 0.0073 mol) and aqueous formaldehyde (2.7 ml, 0.036 mol, 37 percent) in 15 ml acetonitrile was added sodium cyanoborohydride (0.7352 g, 0.0117 mol). After stirring for 15 minutes, the reaction was made acidic by addition of 15 ml glacial acetic acid over a 45 minute period. The solution was made basic by the addition of an aqueous solution of ammonium hydroxide. The basic solution was extracted 3 times with ethyl acetate, the organic layer was then dried using sodium sulfate and concentrated under reduced pressure. Purification on silica gel column chromatography using 9 parts diethyl ether and 1 part triethylamine followed by bulb-to-bulb distillation (80° C. 0.4 mmHg)) to give 2-acetyl-3,8-dimethyl-8-azabicyclo[3.2.1]oct-2-ene as a brownish liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288872
Source datasetuspto-grants-1994_02
ORD IDord-7d822a1cb7fa41b0ae51e3dca314592b
Source noteuspto-grants-1994_02