Phenethylamine → Benzylmethyl(tetrahydropyran-4-yl)amine

Into a similar device to that used in Example 7 were charged 1.38 g (5.0 mmol) of tetrahydropyranyl-4-p-toluenesulfonate synthesized in Example 6 and having a purity of 93% and 3.18 g (26.0 mmol) of benzylmethylamine, and the mixture was reacted at 70° C. for 4 hours and further at 90° C. for 5 hours. After completion of the reaction, the resulting reaction mixture was concentrated under reduced pressure and purified by silica gel column chromatography (Filler: Wako gel C-200 (available from Wako Junyaku Co.), Eluent: chloroform/methanol (=9/1 (volume ratio)) to obtain 0.72 g (yield: 70%) of 4-benzylmethylaminotetrahydropyrane having a purity of 90% (areal percentage according to high performance liquid chromatography) as a pale yellowish liquid.

1. customthe mixture was reacted at 70° C. for 4 hours and further at 90° C. for 5 hours
2. customAfter completion of the reaction
3. customthe resulting reaction mixture
4. concentrationwas concentrated under reduced pressure
5. custompurified by silica gel column chromatography (Filler

ORD record

ord-cb559659f8844425821ffec9d39d59e7

Source dataset

uspto-grants-2003_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06653489B2