Reaktion #46512

ord-1d39fe7923784c69934bc7c2647b99ac

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas poured onto ice water (200 mL)
  2. 2
    workup.STIRRINGstirred until the suspension
  3. 3
    workup.DISSOLUTIONdissolved
  4. 4
    SonstigeThe organic phase was separated
  5. 5
    Trocknendried (MgSO4)
  6. 6
    Einengenconcentrated under vacuum
  7. 7
    SonstigePurification by flash chromatography on silica gel (10% ethyl acetate/hexane)

Vorschrift

SnCl4 (20 mL, 67 mmole) was added over 5 min to a stirred solution of 2-methylbenzo[b]thiophene (5.0 g, 33.7 mmole) in CH2Cl2 (75 mL) at 0° C. under argon. After 15 minutes, dichloromethyl methyl ether (3.7 mL, 41 mmole) was added. The reaction became a yellowish colored suspension. The reaction was allowed to warm to RT and stirred for 16 h, then was poured onto ice water (200 mL). The aqueous mixture was acidified with 1.0 N HCl (100 mL) and stirred until the suspension dissolved. The organic phase was separated, dried (MgSO4), and concentrated under vacuum. Purification by flash chromatography on silica gel (10% ethyl acetate/hexane) gave the title compound (5.83 g, 98%) as a white crystalline solid: 1H NMR (400 MHz, CDCl3) δ 10.38 (s, 1 H), 8.61 (d, J=8.1 Hz, 1 H), 7.77 (d, J=8.0 Hz, 1 H), 7.48 (t, 1 H), 7.39 (t, 1 H), 2.93 (s, 3 H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741339B2uspto-grants-2010_06