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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37586생성일: 2026년 10월 23일

Hydrochloric Acid → 4-Acetyl-2,2-difluoro-1,3-benzodioxole

https://huagongshe.com/ko/reaction/37586

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,2-Difluoro-1,3-benzodioxoleHCID 74103—
반응물N-Methoxy-N-methylacetamideHCID 537505—
반응물Potassium tert-butoxideHCID 23665647—
반응물ButyllithiumHCID 178418339—
반응물HCID 178506008HCID 178506008—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물4-Acetyl-2,2-difluoro-1,3-benzodioxoleHCID 10987257—

반응 조건

온도-10 °C

반응 단계

6.2 g (55 mmol) of potassium tert.-butoxide dissolved in 40 ml of tetrahydrofuran (THF) are added dropwise at -30° C. under argon, over a period of 20 minutes, to a solution of 8.0 g (50 mmol) of 2,2-difluoro-1,3-benzodioxole in 10 ml of THF in a 250 ml 3-necked flask. The mixture is then cooled to -90° C. (methanol/liquid nitrogen), and 35 ml (55 mmol) of n-butyllithium (1.58M in hexane) are added thereto over a period of 30 minutes. The deep red solution of 2,2-difluoro-1,3-benzodioxol-4-yl-potassium is maintained at -78° C. for 20 minutes. Then, 5.2 g (50 mmol) of N-methyl-N-methoxy-acetamide in 20 ml of THF are added thereto over a period of 15 minutes at -78° C. When the dropwise addition is complete, the beige reaction mixture is allowed to warm up to -10° C. and is then hydrolysed with 40 ml of 10% hydrochloric acid. The hydrolysed mixture is extracted three times with 70 ml of diethyl ether each time. The organic solutions are washed three times with 30 ml of 1N HCl each time, dried over Na2SO4 and concentrated in a vacuum rotary evaporator. Upon distillation of the residue, 7.1 g (79%) of the product distil over in the form of a colourless oil at boiling point (b.p.) 114°-116° C./30 mbar.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420301
출처 데이터셋uspto-grants-1995_05
ORD IDord-a993f9e060384978a00251358c75b4bf
출처 메모uspto-grants-1995_05