Methanol → Methyl L-tert-leucinate hydrochloride

To anhydrous methanol (15 mL) at -20° C. under nitrogen was added thionyl chloride (4 mL) dropwise. The solution was allowed to warm to room temperature and then tert-Leucine (4.00 g) was added. The reaction mixture was warmed at 50° C. for 5 hours, re-cooled to -20° C., and then additional thionyl chloride (3 mL) was added dropwise. The reaction mixture was heated an additional 2.5 hours at 50° C. and then concentrated under reduced pressure and chased twice with methanol (15 mL) to afford an amorphous solid. The solid was triturated with ether to afford the title compound in 92% yield. The 300 MHz 1H NMR spectrum was found to be consistent with the proposed structure. MS (DCI/NH3) m/e 146 (M+H)+.

1. temperatureThe reaction mixture was warmed at 50° C. for 5 hours
2. temperaturere-cooled to -20° C.
3. temperatureThe reaction mixture was heated an additional 2.5 hours at 50° C.
4. concentrationconcentrated under reduced pressure
5. customto afford an amorphous solid
6. customThe solid was triturated with ether

ORD-Eintrag

ord-59cf2f824cfa4012ba8c0711d53c8412

Quelldatensatz

uspto-grants-1998_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05837873