反应 #1256739

反应方程式

sulfuric acid

LiAlH4

H2SO4

4-Cyanobenzoic acid

→

4-(aminomethyl)benzyl alcohol

收率 70.6%

4-(Aminomethyl)benzyl alcohol

收率 70.6%

溶剂

ether

反应条件

后处理

1. 1
   workup.ADDITIONwere added dropwise
2. 2
   温度The reaction was heated
3. 3
   温度to reflux for 4 hours
4. 4
   其他The 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
   其他The ether was decanted off the resulting gel
7. 7
   萃取the gel was extracted twice with 600 mL portions of ether
8. 8
   干燥The combined ether fractions were dried over MgSO4
9. 9
   其他evaporated under vacuum

实验过程

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).

来源