Chlorotrimethylsilane → (5S)-5,6-dihydroxy-3-oxohexanoic tert-butyl ester

温度

65 °C

To a suspension of 9.82 g (150 mmol) of zinc dust in 40 mL of tetrahydrofuran was added 1.9 mL (15 mmol) of trimethylsilyl chloride at room temperature, and the mixture was stirred for 30 minutes. To this mixture were added 2.4 mL (10.5 mmol) of tert-butyl α-bromoacetate and 4.27 g (42 mmol) of (S)-β-hydroxy-γ-butyrolactone, and the temperature was increased to 65° C. At the same temperature, 15.3 mL (94.5 mmol) of tert-butyl α-bromoacetate was further added gradually over 30 minutes. After completion of addition, the mixture was further stirred at 65° C. for 30 minutes, at the end of which time the reaction mixture was cooled to room temperature and diluted with 50 mL of water. The reaction mixture was then adjusted to pH 6.8 with 20% aqueous NaOH solution and the precipitated solid was filtered off. The filtrate was extracted with 3 portions of ethyl acetate, 100 mL each, and the organic layers were combined and dehydrated over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure to give a yellow oil. This residue was purified by silica gel column chromatography (Kieselgel 60, product of Merck; hexane:acetone=5:1) to give 2.66 g of (5S)-5,6-dihydroxy-3-oxohexanoic tert-butyl ester (yellow oil). Yield 29%.

1. additionAfter completion of addition
2. stirringthe mixture was further stirred at 65° C. for 30 minutes, at the end of which time the reaction mixture
3. temperaturewas cooled to room temperature
4. filtrationthe precipitated solid was filtered off
5. extractionThe filtrate was extracted with 3 portions of ethyl acetate, 100 mL each
6. distillationThe solvent was then distilled off under reduced pressure
7. customto give a yellow oil
8. customThis residue was purified by silica gel column chromatography (Kieselgel 60, product of Merck; hexane:acetone=5:1)

ORDレコード

ord-1fa056755395410a8769840af876295d

出典データセット

uspto-grants-2006_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07094594B2