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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154774Generated: October 27, 2026

Ammonium Chloride → 1,2,3,4,5,8,8a,9,10,10a-Decahydro-2,3-dimethylene-1,4-epoxy-8-hydroxy-anthracen-5-one

https://huagongshe.com/reaction/1154774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTetrabutylammonium borohydrideHCID 169536—
Reactant1,2,3,4,8a,9,10,10a-Octahydro-2,3-dimethylene-1,4-epoxyanthracene-5,8-dioneHCID 13340977—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product1,2,3,4,5,8,8a,9,10,10a-Decahydro-2,3-dimethylene-1,4-epoxy-8-hydroxy-anthracen-5-oneHCID 524958674%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of 3.38 g of 1,2,3,4,8a,9,10,10a-octahydro-2,3-dimethylene-1,4-epoxyanthracene-5,8dione in 50 ml of methylene chloride and 50 ml of methanol was cooled to -70° C. and treated under nitrogen with 2.04 g of tetra-n-butylammonium borohydride in 10 ml of methylene chloride. The mixture was then stirred at -70° C. for 1.75 hours. After the addition of 100 ml of aqueous ammonium chloride solution, the solution was stirred for a further 1 hour. The phases were separated, the aqueous phase was extracted twice with 50 ml of methylene chloride each time and the combined organic phases were washed with two 100 ml portions of water and subsequently dried over magnesium sulphate. After concentration and recrystallisation, there were obtained 2.52 g (74%) of 1,2,3,4,5,8,8a,9,10,10a-decahydro-2,3-dimethylene-1,4-epoxy-8-hydroxy-anthracen-5-one of melting point 206°-207° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298535
Source datasetuspto-grants-1981_11
ORD IDord-d1aa7d18196a47fc8ad5532cd85cacfd
Source noteuspto-grants-1981_11