반응 #1121735

ord-68f4ba8509d9404bb415fce37f2d937b

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The mixture was concentrated
  2. 2
    기타the residue was partitioned between EtOAc (15 mL) and aqueous saturated ammonium chloride solution (10 mL)
  3. 3
    기타The layers were separated
  4. 4
    추출the aqueous layer was extracted with 2 additional portions of EtOAc (10 mL)
  5. 5
    건조The combined extracts were dried (MgSO4)
  6. 6
    여과filtered
  7. 7
    농축concentrated

실험 절차

TBAF (1.0 M in THF, 0.5 mL, 0.50 mmol, 1.2 equiv) was added in one portion to a dry THF (100 μL) solution of 3-(tert-butyldimethylsilyloxy)-N,N-dimethyl-2-((9Z,12Z)-octadeca-9,12-dienyloxy)propan-1-amine (0.2 g, 0.42 mmol, 1.0 equiv) and the mixture was stirred at room temperature for 2 hours. The mixture was concentrated and the residue was partitioned between EtOAc (15 mL) and aqueous saturated ammonium chloride solution (10 mL). The layers were separated and the aqueous layer was extracted with 2 additional portions of EtOAc (10 mL). The combined extracts were dried (MgSO4), filtered, and concentrated to give crude 3-(dimethylamino)-2-((9Z,12Z)-octadeca-9,12-dienyloxy)propan-1-ol, a thick, beige oil, which was used without further purification.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08545876B1uspto-grants-2013_10