Sodium Hydroxide → 1-((S)-1-benzylpyrrolidin-2-yl)cyclopropanol

温度

-15 °C

First 6.91 mL (23.57 mmol) of titanium (IV) isopropoxide and then 14.3 mL (42.9 mmol, 3 M in diethyl ether) of ethylmagnesium bromide were slowly added dropwise to a solution of 5.0 g (21.43 mmol) of N-benzyl-L-proline ethyl ester in 80 mL of dry diethyl ether which had been cooled to −15° C. and the reaction mixture was stirred for 30 minutes at this temperature. Subsequently at approximately 10° C., 5.4 mL (42.9 mmol) of boron trifluoride-diethyl ether complex were added and the mixture was stirred for a further 75 hours at RT. While cooling, 50 mL of 1M NaOH was added, the mixture was stirred for 1 hours at RT, combined with 100 mL of diethyl ether, and the organic phase was separated off and dried over sodium sulfate. After the desiccant and solvent had been eliminated, the residue was purified by chromatography (silica gel, EtOAc). Yield: 0.745 g (16% of theoretical); C14H19NO (M=217.307); calc.: molpeak (M+H)+: 218; found: molpeak (M+H)+: 218; Rf value: 0.17 (silica gel, EtOAc).

1. additionSubsequently at approximately 10° C., 5.4 mL (42.9 mmol) of boron trifluoride-diethyl ether complex were added
2. stirringthe mixture was stirred for a further 75 hours at RT
3. temperatureWhile cooling
4. stirringthe mixture was stirred for 1 hours at RT
5. customthe organic phase was separated off
6. dry with materialdried over sodium sulfate
7. customthe residue was purified by chromatography (silica gel, EtOAc)

ORDレコード

ord-fab0ef437fc64a3ca983929e4aef59eb

出典データセット

uspto-grants-2009_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07592358B2