Réaction #53854

Équation de réaction

KHSO4

iodomethane

trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester

NaH

→

trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester

Rendement 84.0%

Solvants

water Et2O

DMF

Conditions de réaction

Traitement

1. 1
   Températurewarmed up to RT over night
2. 2
   TempératureThe reaction is cooled
3. 3
   LavageThe organic phase was washed with aqueous 10% NaCl
4. 4
   Séchagedried over Na2SO4
5. 5
   Autreevaporated
6. 6
   Autrepurified by flash silica gel column (CH2Cl2/EtOAc 9:1 to 1:1)

Mode opératoire

A solution of 24.18 g (82 mmol) of trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester in 80 ml of DMF was treated at 0° C. with 5.37 g (123 mmol) of 55% NaH in small portions. The reaction was stirred for 1 h at 0° C., then treated slowly (20 min) with 40.9 ml (656 mmol) iodomethane and warmed up to RT over night. The reaction is cooled and neutralized with aqueous 10% KHSO4 and poured into water/Et2O (3×). The organic phase was washed with aqueous 10% NaCl, dried over Na2SO4 evaporated and purified by flash silica gel column (CH2Cl2/EtOAc 9:1 to 1:1) to yield 20.69 g (84%) of trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester, MS: 301 (MH+).

Source