반응 #2075738

ord-312a03426be54f05abfaf82ed0fc22ff

반응 방정식

BrP(Br)Br
PBr3
CC(C)(C)OC(=O)n1ccc2c(CO)cccc21
tert-butyl 4-(hydroxymethyl) 1H-1-indolecarboxylate
CC(C)(C)OC(=O)n1ccc2c(CO)cccc21
N-Boc-4-hydroxymethyl indole
O=C([O-])O.[Na+]
NaHCO3
CC(C)(C)OC(=O)n1ccc2c(CBr)cccc21
tert-butyl 4-(bromomethyl)-1H-1-indolecarboxylate
수율 84.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONafter the addition
  2. 2
    추출extracted with ethyl acetate (3×80 mL)
  3. 3
    추출The combined extract
  4. 4
    세척was washed sequentially with water (80 mL), and brine (80 mL)
  5. 5
    건조dried (MgSO4)
  6. 6
    여과filtered
  7. 7
    농축finally concentrated

실험 절차

PBr3 (2.4 mL. 25.8 mmol) was added dropwise at 0° C. under nitrogen to a stirred solution of tert-butyl 4-(hydroxymethyl) 1H-1-indolecarboxylate 6 (6.0 g, 24.3 mmol) in ether (80 mL) and CH2Cl2 (20 mL) under nitrogen. The reaction was completed 30 minutes after the addition. The mixture was poured into a cold aqueous NaHCO3 solution (100 mL) and extracted with ethyl acetate (3×80 mL). The combined extract was washed sequentially with water (80 mL), and brine (80 mL), then dried (MgSO4), filtered, and finally concentrated to provide tert-butyl 4-(bromomethyl)-1H-1-indolecarboxylate 7 (6.3 g, 84%) as an oil which was immediately taken to the next step.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07642231B2uspto-grants-2010_01