تفاعل #1833273

معادلة التفاعل

NaOH

1-((2-methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzene

Intermediate K

1-((2-methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzene

HCl

→

(trans)-2-(4-((2-methoxyethoxy)methoxy)phenyl)cyclopropanamine

المردود 73.0%

المذيبات

i-PrOH

ظروف التفاعل

المعالجة

1. 1
   ترشيحfiltered through a pad of celite, that
2. 2
   غسيلwas washed with 10 mL of methanol
3. 3
   تركيزThe filtrate was concentrated
4. 4
   workup.ADDITION15 mL of water were added
5. 5
   استخلاصextracting with CH2Cl2 (3×15 mL)
6. 6
   غسيلthe organic layers were washed with brine (25 mL)
7. 7
   تجفيفdried over anhydrous Na2SO4
8. 8
   ترشيحfiltered
9. 9
   أخرىAfter removal of the solvent
10. 10
    أخرىthe crude product was purified by column chromatography on silica gel (2-5% MeOH/CH2Cl2)

الإجراء التجريبي

Zn dust (0.99 g, 15.1 mol) was added in small portions, over a period of 20 min, to a vigorously stirred solution of 1-((2-methoxyethoxy)methoxy)-4-((trans)-2-nitrocyclopropyl)benzene (Intermediate K, 0.40 g, 1.51 mmol) in i-PrOH (15 mL) and HCl (5.6 mL of 2.7 N aqueous solution, 15.1 mmol). After 16 h, the mixture was basified with NaOH (10% aqueous solution, 10 mL) and filtered through a pad of celite, that was washed with 10 mL of methanol. The filtrate was concentrated and 15 mL of water were added, extracting with CH2Cl2 (3×15 mL); the organic layers were washed with brine (25 mL), dried over anhydrous Na2SO4 and filtered. After removal of the solvent, the crude product was purified by column chromatography on silica gel (2-5% MeOH/CH2Cl2) affording 0.26 g of (trans)-2-(4-((2-methoxyethoxy)methoxy)phenyl)cyclopropanamine [Rf=0.1 (5% MeOH/CH2Cl2), white solid, 73% yield].

المصدر