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HRID 388744Erstellt: 24. Oktober 2026

Acetic Acid → (1s,3s,5r,6s)-5-{[Tert-butyl(dimethyl)silyl]oxy}-6-methyl-7-oxabicyclo[4.1.0]heptan-3-ol

https://huagongshe.com/de/reaction/388744

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPotassium CarbonateHCID 11430—
Edukt(1s,3s,5r,6s)-5-{[Tert-butyl(dimethyl)silyl]oxy}-6-methyl-7-oxabicyclo[4.1.0]hept-3-yl acetateHCID 87629193—
LösungsmittelMethanolHCID 887—
Produkt(1s,3s,5r,6s)-5-{[Tert-butyl(dimethyl)silyl]oxy}-6-methyl-7-oxabicyclo[4.1.0]heptan-3-olHCID 8762883098%

Reaktionsschritte

The compound of Example 16C (9.20 g, 30.6 mmol) was dissolved in 105 mL of methanol. K2CO3 (10.1 g, 72.1 mmol, 2.35 equivalents) was added and the reaction mixture was stirred at ambient temperature for 2 hours. 6.60 mL (115 mmol, 3.77 equivalents) of acetic acid were added to the reaction mixture; after mixing for 10 minutes, the solids were filtered off and rinsed with 40 mL of methanol. The combined filtrate and rinses were concentrated to a residue which was mixed with 106 mL of water. The layers were separated, and the aqueous layer was extracted three times with 50 mL of ethyl acetate. The combined organic layers were washed twice with 45 mL of brine, dried over MgSO4, filtered and concentrated to afford the titled compound (7.72 g, 98%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08377913B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-2613d346a3a24dd887853b5dc7d0b75a
Quellennotizuspto-grants-2013_02