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Tetrahydrofuran → HCID 22805384, Verbindung

HRID 1706628
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1706628
[CH3:1][C@@:2]1([C:8](O)=[O:9])[CH2:6][CH2:5][C:4](=[O:7])[O:3]1.O1CCCC1>O>[OH:9][CH2:8][C@@:2]1([CH3:1])[O:3][C:4](=[O:7])[CH2:5][CH2:6]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 8028TetrahydrofuranHCID 53249432(2S)-2-Methyl-5-oxooxolane-2-carboxylic acid

Produkt 1

HCID 22805384HCID 22805384, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To a solution of 14.8 g. (102.7 mmol) of (S)-(-)-2-methyl-5-oxotetrahydro-2-furoic acid mp 84°-87° C.; [α]25D-16.56° in 70 ml. of dry tetrahydrofuran (THF) was added 10.1 ml. (8.1 g.; 106.7 mmol) of borane-methyl sulphide complex, dropwise, with stirring over a 0.5 hr. period. Occasional ice-bath cooling was employed to maintain the internal temperature below 30°. After stirring at room temperature for 1.5 hr., the reaction mixture was cautiously decomposed by the dropwise addition of 6.2 ml. of H2O. The mixture was then concentrated under water aspirator pressure and the residue was taken up in ethyl acetate and filtered. The solids were washed thoroughly with ethyl acetate and filtered. The solids were washed thoroughly with ethyl acetate and the filtrate and washes were combined and concentrated in vacuo giving (S)-(+)-5-(hydroxymethyl)-5-methyldihydro-2(3H)-furanone as a colorless oil (13.6 g.) which was used without further purification.

Aufarbeitung

  1. temperatureOccasional ice-bath cooling
  2. temperatureto maintain the internal temperature below 30°
  3. stirringAfter stirring at room temperature for 1.5 hr
  4. addition, the reaction mixture was cautiously decomposed by the dropwise addition of 6.2 ml
  5. concentrationThe mixture was then concentrated under water aspirator pressure
  6. filtrationfiltered
  7. washThe solids were washed thoroughly with ethyl acetate
  8. filtrationfiltered
  9. washThe solids were washed thoroughly with ethyl acetate
  10. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-80644101c3194e62920df8a677b6291f
Quelldatensatz
uspto-grants-1980_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04208331

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