반응 #1256739

ord-64464a6d547d4824ade147ac1fd700a9

반응 방정식

O=S(=O)(O)O
sulfuric acid
[Al+3].[H-].[H-].[H-].[H-].[Li+]
LiAlH4
O=S(=O)(O)O
H2SO4
N#Cc1ccc(C(=O)O)cc1
4-Cyanobenzoic acid
NCc1ccc(CO)cc1
4-(aminomethyl)benzyl alcohol
수율 70.6%
NCc1ccc(CO)cc1
4-(Aminomethyl)benzyl alcohol
수율 70.6%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwere added dropwise
  2. 2
    온도The reaction was heated
  3. 3
    온도to reflux for 4 hours
  4. 4
    기타The reaction was quenched on ice with 215 mL of water
  5. 5
    workup.ADDITIONfollowed by the addition of 80 g of NaOH in 650 mL of water
  6. 6
    기타The ether was decanted off the resulting gel
  7. 7
    추출the gel was extracted twice with 600 mL portions of ether
  8. 8
    건조The combined ether fractions were dried over MgSO4
  9. 9
    기타evaporated under vacuum

실험 절차

Adapting the procedure described by Keppler et al., Nature Biotechnology 21, 86-89 (2003), 1.5 L of 0.5 M LiAlH4 were chilled on ice and 22 mL of concentrated H2SO4 were added dropwise. 4-Cyanobenzoic acid (10) 20 g (136 mmol) was suspended in 120 mL of ether and this was added dropwise to the sulfuric acid. The reaction was heated to reflux for 4 hours. The reaction was quenched on ice with 215 mL of water followed by the addition of 80 g of NaOH in 650 mL of water. The ether was decanted off the resulting gel and the gel was extracted twice with 600 mL portions of ether. The combined ether fractions were dried over MgSO4 and evaporated under vacuum to give 13.1 g (96 mmol) of 4-(aminomethyl)benzyl alcohol (11) as a clear oil. 1H NMR (CDCL3/TMS) δ=1.95 (broad s, 3H, —OH and —NH2, exchangeable with D2O), 3.86 (s, 2H, —CH2—NH2), 4.68 (s, 2H, —CH2—OH), 7.30 (m, 4H, aromatic).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07825096B2uspto-grants-2010_11