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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1439846생성일: 2026년 10월 27일

Hydrochloric Acid → 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine

https://huagongshe.com/reaction/1439846

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물Sodium borohydrideHCID 4311764—
반응물2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 13690761—
용매TetrahydrofuranHCID 8028—
생성물2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 1898441691.2%

반응 단계

To a mixture of 2-(4-fluorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine (4.0 g), sodium borohydride (2.91 g) and tetrahydrofuran (100 ml) is added dropwise with stirring boron trifluoride etherate complex (12. 5 ml) at room temperature, and the mixture is refluxed for 1.5 hour. After cooling, to the mixture is added dropwise 10% hydrochloric acid (35 ml), and the mixture is further refluxed for one hour. The reaction mixture is poured into ice water and made alkaline with potassium carbonate and extracted with ethyl acetate. The ethyl acetate layer is washed, dried and distilled to remove the solvent. The residue is recrystallized from isopropyl ether to give 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (3.45 g, yield 91%) as crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05496815
출처 데이터셋uspto-grants-1996_03
ORD IDord-488b059e0af749058875b4b319e2edcb
출처 메모uspto-grants-1996_03