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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850715Generated: November 3, 2026

Methanol → (1RS,2SR,6RS)-2-Hydroxymethyl-8-azabicyclo[4.3.0]non-4-ene

https://huagongshe.com/reaction/850715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactantethyl (1RS,2RS,6RS)-9-oxo-8-azabicyclo[4.3.0]non-4-ene-2-carboxylateHCID 54398625—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(1RS,2SR,6RS)-2-Hydroxymethyl-8-azabicyclo[4.3.0]non-4-eneHCID 19364990—

Reaction Steps

5.2 g (25 mmol) of ethyl (1RS,2RS,6RS)-9-oxo-8-azabicyclo[4.3.0]non-4-ene-2-carboxylate (product A from Example K.2.) are dissolved in 50 ml of tetrahydrofuran under a nitrogen atmosphere and 130 ml of a 1.5 molar di(isobutyl)aluminium hydride solution (195 mmol) are subsequently added dropwise. The solution is heated under reflux for 16 h. After the reaction is complete, 60 ml of methanol, 30 ml of tert-butyl methyl ether and 10 ml of water are added dropwise successively and filtration with suction is then carried out in the presence of tonsil. The suction filter residue is stirred twice with a mixture of ethanol/conc. ammonia/water (10:1:1) and filtered off with suction once again. The combined filtrates are concentrated and the crude product is purified by chromatography (eluent: dichloromethanel-methanol/conc. ammonia 2:4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06018054
Source datasetuspto-grants-2000_01
ORD IDord-1caa9648b4ed44fead0a579ceb6c8b2a
Source noteuspto-grants-2000_01