In the Gabriel synthesis of primary amines, N-potassiophthalimide is used as a source of the nitrogen atom. Complete the synthesis reactions by drawing the missing structures. Ignore inorganic counterions. NH2 N K* DMF Step 1 Product NaOH (xs) H20, heat Step 2 Product Br KBr

In the Gabriel synthesis of primary amines, N-potassiophthalimide is used as a source of the nitrogen atom. Complete the synthesis reactions by drawing the missing structures. Ignore inorganic counterions. NH2 N K* DMF Step 1 Product NaOH (xs) H20, heat Step 2 Product Br KBr

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section: Chapter Questions

Problem 19.69P

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Draw the Step 2 product.
Draw the Step 1 product.
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H.
OH,
OH,
N

In the Gabriel synthesis of primary amines, N-potassiophthalimide is used as a source of the nitrogen atom. Complete the
synthesis reactions by drawing the missing structures. Ignore inorganic counterions.
NH2
N K*
DMF
Step 1
Product
NaOH (xs)
H2O, heat
Step 2
Product
Br
KBr

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