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2-methylspiro[3.3]heptane-2-carboxylic acid → HCID 20320778, Verbindung

HRID 866395
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 866395
[CH3:1][C:2]1([C:9]([OH:11])=O)[CH2:5][C:4]2([CH2:8][CH2:7][CH2:6]2)[CH2:3]1.[CH3:12][Li]>CCOCC>[CH3:1][C:2]1([C:9](=[O:11])[CH3:12])[CH2:3][C:4]2([CH2:6][CH2:7][CH2:8]2)[CH2:5]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 203207772-methylspiro[3.3]heptane-2-carboxylic acidHCID 178418348HCID 178418348, Verbindung

Produkt 1

HCID 20320778HCID 20320778, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel2×

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

A solution of 5.0 g (33.0 mmol) 2-methylspiro[3.3]heptane-2-carboxylic acid in 33.0 ml of dry ether was stirred under argon at 0° C and 47.6 ml (74.3 mmol) of 1.56 M methyl lithium in ether added dropwise. The reaction mixture was allowed to warm to 25° C and was stirred for 3.0 hr. The reaction mixture was cooled to -20° C and quenched by addition of 10% aqueous HCl. The layers were separated and the aqueous layer extracted with ether. The combined organic layers were washed with saturated aqueous sodium bicarbonate and brine, then dried (MgSO4), filtered, and evaporated in vacuo to afford 2-methyl-2-acetylspiro[3.3]heptane as a light yellow oil (4.91 g 98%).

Aufarbeitung

  1. temperatureThe reaction mixture was cooled to -20° C
  2. customquenched by addition of 10% aqueous HCl
  3. customThe layers were separated
  4. extractionthe aqueous layer extracted with ether
  5. washThe combined organic layers were washed with saturated aqueous sodium bicarbonate and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-50122c90e0b540f0acefcad7db2d1dc0
Quelldatensatz
uspto-grants-1978_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04098823

Notizen zur Reaktion

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