L-Tryptophan → benzyloxycarbonyl-L-tryptophan

Temperature

0 °C

To a suspension of tryptophan (20.08 g; 98.32 mmol) in H2O, cooled to 0° C., was added 1N NaOH (98 mL; 98 mmol) and the solution became clear. Maintaining the temperature at 0° C., 1N NaOH (108 mL; 108 mmol) and benzyl chloroformate (CBZCl, commercial product) (15.38 mL; 107.7 mmol) were simultaneously dropped in the reaction mixture. After the addition the mixture was kept at 0° C. for 30 min and then allowed to rise to r. t. The reaction was monitored by HPLC (Chromatographic method of Example 3, A). After further 3 h the pH was corrected to 9.5 by addition of 1N NaOH and the mixture was washed with Et2O (200 mL). The aqueous layer was acidified to pH 2 using 2N HCl and the precipitate was filtered through a G3 septum, washed with cold water (2×200 mL) and dried over P2O5 under vacuum (2 kPa). N-[(Phenylmethoxy)carbonyl]-L-tryptophan (33.96 g) was obtained and used in the following step without further purification.

1. temperatureMaintaining the temperature at 0° C.
2. additionAfter the addition the mixture
3. washthe mixture was washed with Et2O (200 mL)
4. filtrationthe precipitate was filtered through a G3 septum
5. washwashed with cold water (2×200 mL)
6. dry with materialdried over P2O5 under vacuum (2 kPa)

ORD record

ord-9be16ca5aa7f44bc924801c436cb112a

Source dataset

uspto-grants-2002_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06403055B1