Methanol → trans-Decahydroisoquinoline

A solution of 800 mg of N-methyl-4a-(m-methoxyphenyl)-trans-decahydroisoquinoline (3.09 mmoles) in 30 ml of methylene chloride was added in portions to an ice-cold solution of 0.59 ml (1.55 g, 6.18 mmoles) of boron tribromide in 15 ml of methylene chloride. The solution, protected under nitrogen, was kept overnight at 25° C. Methanol (5 ml) was then added and the solution evaporated. The residue was treated with 15 ml of 5 N aqueous sodium hydroxide and the mixture stirred for 15 minutes. Ether (50 ml) was added and the bilayer mixture stirred for 2 hours. The aqueous and ether layers were finally separated and the aqueous portion saturated with carbon dioxide. The resulting solid precipitate was extracted with ether and the extract concentrated to give 680 mg of N-methyl-4a-(m-hydroxyphenyl)-trans-decahydroisoquinoline, mp 195°-205° C.

1. customthe solution evaporated
2. additionThe residue was treated with 15 ml of 5 N aqueous sodium hydroxide
3. additionEther (50 ml) was added
4. stirringthe bilayer mixture stirred for 2 hours
5. customThe aqueous and ether layers were finally separated
6. extractionThe resulting solid precipitate was extracted with ether
7. concentrationthe extract concentrated
8. customto give 680 mg of N-methyl-4a-(m-hydroxyphenyl)-trans-decahydroisoquinoline, mp 195°-205° C.

ORD record

ord-a17c55ec2dbd4b41b596bd72eeee25f8

Source dataset

uspto-grants-1983_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04419517