Reaktion #6644

ord-964ba96c58d94d2ea992b45e7a732b3b

Reaktionsgleichung

CC1(C)CC(C)(C)c2ccccc2O1
2,2,4,4-tetramethylchroman
CC1(C)CC(C)(C)c2ccccc2O1
Compound 84
CC1(C)CC(C)(C)c2ccccc2O1
2,2,4,4-tetramethylchroman
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
CC(=O)Cl
acetyl chloride
CC(=O)c1ccc2c(c1)C(C)(C)CC(C)(C)O2
title compound
CC(=O)c1ccc2c(c1)C(C)(C)CC(C)(C)O2
2,2,4,4-Tetramethyl-6-acetyl-chroman

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added, under nitrogen
  2. 2
    SonstigeThe cooling bath was then removed
  3. 3
    TemperaturThe mixture was then cooled again in an ice bath
  4. 4
    workup.ADDITIONtreated with 25 ml of conc. HCl
  5. 5
    FiltrationThe mixture was then filtered
  6. 6
    Waschenthe residue washed with methylene chloride
  7. 7
    EinengenThe filtrate was concentrated in vacuo
  8. 8
    Sonstigethe resultant residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes)

Vorschrift

To an ice bath cooled solution of 2 g (10.53 mmol) of 2,2,4,4-tetramethylchroman (Compound 84) in 25 ml of nitromethane was added, under nitrogen, 941 mg (11.99 mmol) of acetyl chloride followed by 1.59 g (11.92) mmol) of aluminum chloride. The cooling bath was then removed and the mixture stirred at room temperature for 16 h. The mixture was then cooled again in an ice bath and treated with 25 ml of conc. HCl. The mixture was then filtered and the residue washed with methylene chloride. The filtrate was concentrated in vacuo and the resultant residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes) to give the title compound as a yellow oil. PMR (CDCl3): δ 1.38 (6H, s), 1.39 (6H, s), 1.87 (2H, s), 2.56 (3H, s), 6.83 (1H, d, J~8.7 Hz), 7.71 (1H, dd, J~8.7 Hz, 2.1 Hz), 7.98 (1H, d, J~2.1 Hz). MS exact mass, m/e 232.1468 (calcd. for C13H20O2, 232.1464).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05248777uspto-grants-1993_09