Naphthalene → 3,3-Dimethyl-1,2,3,4-tetrahydroisoquinoline

HRID 2393763Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2393763
C1C2C(=CC=CC=2)C=CC=1.[Na].C1(C)C(S([N:21]2[C:30]([CH3:32])([CH3:31])[CH2:29][C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[CH2:22]2)(=O)=O)=CC=CC=1>C(COC)OC.COCOC>[CH3:31][C:30]1([CH3:32])[CH2:29][C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH2:22][NH:21]1

Komponenten

6

Versuchsvorschrift

To a stirred solution of naphthalene (5.8 g, 0.045 mol) in dimethoxyethane (50 mL) was added sodium metal (1.09 g, 0.039 mol.). The mixture was allowed to stir for four (4) hours until a dark green color persisted. To this was added of N-toluenesulfonyl-3,3-dimethyl-1,2,3,4-tetrahydroisoquinoline (5.0 g, 0.016 mol.) in 20 mL of dimethoxymethane. The reaction was monitored by gas chromatography. When the reaction was complete (≈2 hours), the mixture was quenched with saturated sodium chloride (70 mL). The mixture was partitioned between ethyl acetate (250 mL) and 10% HCL (250 mL) and the organic layer was discarded. 10% Sodium hydroxide was added to the aqueous layer until a pH=7 was obtained. The aqueous layer was further extracted over methylene chloride (2×100 mL), dried over magnesium sulfate, filtered and concentrated (25° C./150 torr) to produce 2.2 g (86%) of 3,3-dimethyl-1,2,3,4-tetrahydroisoquinoline.

Aufarbeitung

  1. custom(≈2 hours)
  2. customthe mixture was quenched with saturated sodium chloride (70 mL)
  3. customThe mixture was partitioned between ethyl acetate (250 mL) and 10% HCL (250 mL)
  4. addition10% Sodium hydroxide was added to the aqueous layer until a pH=7
  5. customwas obtained
  6. extractionThe aqueous layer was further extracted over methylene chloride (2×100 mL)
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated (25° C./150 torr)

Quellen und Nachweise

ORD-Eintrag
ord-bbc5d5d97eb746e68fb48c9c8d11df52
Quelldatensatz
uspto-grants-1998_09
Patentnummer
US05808071

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