Hydrochloric Acid → Spiro[indene-1,4'-piperidine] hydrochloride

HRID 1110038Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1110038
C(OC([N:8]1[CH2:13][CH2:12][C:11]2([C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:22]>C(OCC)(=O)C>[ClH:22].[NH:8]1[CH2:13][CH2:12][C:11]2([C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)[CH2:10][CH2:9]1

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 3653579Tert-butyl Spiro[indene-1,4'-piperidine]-1'-carboxylate

Produkt 1

HCID 22509344Spiro[indene-1,4'-piperidine] hydrochlorideAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A solution of 1'-(tert-butyloxycarbonyl)spiro [indene-1,4'-piperidine] (3.0 g, 0.011 mol) in ethyl acetate (150 ml) was stirred at 0° C., and treated with hydrogen chloride for 30 minutes. The mixture was then evaporated to dryness, ethyl acetate (100 ml) was added, then removed in vacuo three times. The residue was stirred with anhydrous ether (200 ml), and the solid filtered off, to give spiro[indene-1,4'-piperidine] hydrochloride (2.3 g, 99%) as a pale yellow solid. The product was not purified further.

Aufarbeitung

  1. customThe mixture was then evaporated to dryness, ethyl acetate (100 ml)
  2. additionwas added
  3. customremoved in vacuo three times
  4. filtrationthe solid filtered off

Quellen und Nachweise

ORD-Eintrag
ord-ad79964c21e64bd3b773478810b12fed
Quelldatensatz
uspto-grants-1994_06
Patentnummer
US05324733

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