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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27296생성일: 2026년 10월 24일

Hydrochloric Acid → 3-Ethyl-1-methylcyclobutane-1-carboxylic acid

https://huagongshe.com/ko/reaction/27296

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl iodideHCID 6328—
반응물DiisopropylamineHCID 7912—
반응물Cyclobutanecarboxylic acid, 3-ethyl-HCID 47796—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물3-Ethyl-1-methylcyclobutane-1-carboxylic acidHCID 23344521109.9%

반응 단계

A solution of 19.9 ml (140 mmol) of dry diisopropylamine in 100 ml of dry tetrahydrofuran was stirred in under an argon atmosphere and 63.6 ml (140 mmol) of a solution of n-butyllithium (2.2 M) in hexane was added dropwise thereto while maintaining the temperature below about 5° C. The resultant mixture was then stirred for 15 min with ice-bath cooling. A solution of 8.2 g (64 mmol) of 3-ethylcyclobutanecarboxlic acid (prepared in Example 1E) in 15 ml of dry tetrahydrofuran was added dropwise to the reaction mixture and stirred with cooling for 15 min. Methyl iodide (4.36 ml, 70 mmol) was added to the reaction mixture dropwise and the resultant mixture was stirred without cooling for 2 hr. The mixture was then stirred with ice-methanol bath cooling as 10% hydrochloric acid was added dropwise until the resultant aqueous phase was acidic (about 25 ml was used). The aqueous phase was separated and extracted twice with ether. The combined ether extract was dried over anhydrous magnesium sulfate and the solvent removed in vacuo to yield 10 g of the title compound having the following physical characteristics:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04220795
출처 데이터셋uspto-grants-1980_09
ORD IDord-0ac1b8437f414919bc2f11d7d52ae2d1
출처 메모uspto-grants-1980_09