Reaktion #1483073

ord-e410c1ae0b304bf3a7c1665c5671f278

Reaktionsgleichung

O
water
CC(=O)Cl
acetyl chloride
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
COC(=O)c1ccc2cc[nH]c2c1
1H-indole-6-carboxylic acid methyl ester
COC(=O)c1ccc2c(C(C)=O)c[nH]c2c1
3-acetyl-1H-indole-6-carboxylic acid methyl ester
Ausbeute 99.7%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    Extraktionthis was extracted with ethyl acetate (300 mL)
  3. 3
    TrocknenThe organic layer was dried (MgSO4)
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated

Vorschrift

To a solution of acetyl chloride (0.23 mL, 3.3 mmole) and aluminum chloride (0.88 g, 6.6 mmol) in methylene chloride (30 mL) was added 1H-indole-6-carboxylic acid methyl ester (0.53 g, 3.0 mmol). After stirring 1 hr at room temperature water (300 mL) was added and then this was extracted with ethyl acetate (300 mL). The organic layer was dried (MgSO4), filtered and concentrated to collect 0.65 g (99% yield) of 3-acetyl-1H-indole-6-carboxylic acid methyl ester a light yellow solid. 1H NMR (300 MHz, DMSO) δ 12.27 (s, 1H), 8.52 (s, 1H), 8.24 (d, 1H, J=8.2 Hz), 8.08 (d, 1H, J=1.0 Hz), 7.78 (dd, 1H, J=8.2, 1.0 Hz), 3.86 (s, 3H), 2.47 (s, 3H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08900565B2uspto-grants-2014_12