Reaction #10708

ord-519add250e7d4ab9915edef34623bdcd

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherpurified to a purity of 99.69%
  2. 2
    Othera specific rotation of −100°
  3. 3
    Otherat 25° C.

Procedure

Chiral 2-n-hexyl-2,3-dihydro-thieno[3,4-b][1,4]dioxine was synthesized by transetherification of 3,4-dimethoxythiophene with (S)-1,2-octanediol and purified to a purity of 99.69% as described in INVENTION EXAMPLE 1. It was characterized by GC-MS and 1H-NMR-spectroscopy, and exhibited a specific rotation of −100° at 25° C. and 436 nm in hexane.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07094865B2uspto-grants-2006_08