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Ch. 15 - Reactions of Carboxylic Acids and Carboxylic Acid Derivatives
Bruice - Organic Chemistry 8th Edition
Bruice8th EditionOrganic ChemistryISBN: 9780135213711당신이 사용하는 게 아니라요?교과서 변경
15장, 문제 38d

What alkyl bromide would you use in a Gabriel synthesis to prepare each of the following amines?
d. cyclohexylamine

검증된 단계별 안내
1
Understand the Gabriel synthesis: It is a method used to prepare primary amines by reacting a phthalimide anion with an alkyl halide, followed by hydrolysis or hydrazinolysis to release the amine.
Identify the target amine: The target amine in this case is cyclohexylamine, which has the structure C₆H₁₁NH₂. This means the alkyl group attached to the nitrogen is a cyclohexyl group.
Determine the required alkyl bromide: In the Gabriel synthesis, the alkyl bromide provides the alkyl group that will eventually be attached to the nitrogen. Therefore, the alkyl bromide should have a cyclohexyl group attached to the bromine atom. The structure of the alkyl bromide would be cyclohexyl bromide (C₆H₁₁Br).
Write the reaction sequence: The phthalimide anion (generated by treating phthalimide with a strong base) reacts with cyclohexyl bromide in an SN2 reaction to form an N-alkylphthalimide intermediate.
Complete the synthesis: The N-alkylphthalimide intermediate is then hydrolyzed (using aqueous acid or base) or treated with hydrazine to release the primary amine, cyclohexylamine, as the final product.

비슷한 문제에 대한 검증된 영상 답변:

이 영상 해법은 위 문제에 도움이 된다고 튜터들이 추천한 것입니다.
영상 길이:
2m

주요 개념

질문에 올바르게 답하기 위해 반드시 이해해야 하는 핵심 개념들은 다음과 같습니다.

Gabriel Synthesis

Gabriel synthesis is a method used to prepare primary amines from alkyl halides. It involves the use of phthalimide, which reacts with a base to form a phthalimide salt. This salt then undergoes nucleophilic substitution with an alkyl halide, leading to the formation of the desired amine after hydrolysis. This method is particularly useful for avoiding the formation of secondary or tertiary amines.
추천 영상:
04:53
General Reaction

Alkyl Bromides

Alkyl bromides are organic compounds containing a bromine atom attached to an alkyl group. They are commonly used as electrophiles in nucleophilic substitution reactions due to the polar C-Br bond, which makes the carbon susceptible to attack by nucleophiles. In the context of Gabriel synthesis, the choice of alkyl bromide is crucial as it determines the structure of the resulting amine.
추천 영상:
가이드 코스
0:53
Peptide Sequencing: Partial Hydrolysis with Cyanogen Bromide Concept 1

Cyclohexylamine

Cyclohexylamine is a primary amine derived from cyclohexane, characterized by the presence of an amine group (-NH2) attached to a cyclohexyl group. In Gabriel synthesis, to produce cyclohexylamine, one would need to use a suitable alkyl bromide that can provide the cyclohexyl group. The correct choice of alkyl bromide ensures that the final product is a primary amine, which is essential for the desired outcome.