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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477500생성일: 2026년 10월 25일

Cyclopropanecarbonyl chloride → HCID 14819887, 화합물

https://huagongshe.com/reaction/477500

반응식

참여 물질

역할이름HCID투입량
반응물Cyclopropanecarbonyl chlorideHCID 77637—
반응물5-MethylisoxazoleHCID 79833—
반응물Lithium diisopropylamideHCID 2724682—
반응물LithiumHCID 3028194—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물HCID 14819887HCID 1481988729.9%

반응 조건

온도-78 °C

반응 단계

n-Buyllithium (19.44 ml, 52.5 mmole of a 2.7 M solution in hexane) was added at -15° C. to a solution of diisopropylalmine (5.31g, 52.5 mmole) in 80 ml of dry THF. After 10 min the cooling bath was lowered to -70° C. and 5-methylisoxazole (4.15 g, 50 mmoles) was added to the lithium diidopropylalmine (LDA) solution followed in 30 min by the dropwise addition of cyclopropanecarboxylic acid chloride (5.33 g, 50 mmoles) in 15 ml of THF. The reaction mixture was then stirred at -78° C. for 30 min and at ambient temperature for 2 h. The solvents were evaporated and the residue was partitioned between ether, 30 ml of water and 13 ml of 4 N NaOH. The aqueous layer was separated, acidified with 6 N HCl and extracted with two portions of ether. The extracts were dried and evaporated to a slushy solid that was cchromatographed on 100 g of silica gel using methylene chloride-Skellysolve B (95:5). The appropriate fractions were combined and concentrated to yield 2.26 g of the title compound as a yellow-tinted solid, mp 62°-63.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04888357
출처 데이터셋uspto-grants-1989_12
ORD IDord-09ac9aefe91141aa93355a3918e89440
출처 메모uspto-grants-1989_12