Water → 2-(2,3-Dihydro-1,4-benzodioxin-6-yl)ethan-1-ol
Reaktionsgleichung
B.C1COCC1.[O:7]1[CH2:12][CH2:11][O:10][C:9]2[CH:13]=[C:14]([CH2:17][C:18](O)=[O:19])[CH:15]=[CH:16][C:8]1=2.O>C1COCC1>[O:7]1[CH2:12][CH2:11][O:10][C:9]2[CH:13]=[C:14]([CH2:17][CH2:18][OH:19])[CH:15]=[CH:16][C:8]1=2Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
BH3.THF (44 mL, 44 mmol, 1 M/THF) was added to a 0° C. solution of 2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)acetic acid (3.419 g, 17.6 mmol) in THF (8.8 mL). The reaction was allowed to warm to room temperature and after 2 h, 20 mL H2O was added slowly by syringe. The resulting mixture was extracted with ethyl acetate, the organic portion was washed with brine, and then was dried (Na2SO4), filtered and evaporated. Purification by flash chromatography (ethyl acetate/hexanes) gave the title compound (3.059 g, 99%).
Aufarbeitung
- extractionThe resulting mixture was extracted with ethyl acetate
- washthe organic portion was washed with brine
- dry with materialwas dried (Na2SO4)
- filtrationfiltered
- customevaporated
- customPurification by flash chromatography (ethyl acetate/hexanes)
Quellen und Nachweise
- ORD-Eintrag
- ord-cc51561050704db3ba33c61cfc045b75
- Quelldatensatz
- uspto-grants-2016_07
- Patentnummer
- US09394273B2
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