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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254815생성일: 2026년 10월 26일

Dimethylformamide → N,N,N',N'-Tetramethylazodicarboxamide

https://huagongshe.com/reaction/254815

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물2,2-DimethylpropanehydrazideHCID 545147—
용매DichloromethaneHCID 6344—
생성물N,N,N',N'-TetramethylazodicarboxamideHCID 427861%

반응 단계

To the solution of acid (63) (330 mg, 0.74 mmol) in CH2Cl2 (10 mL) was added oxalyl chloride (77 μL, 0.88 mmol) and the catalytic amount of DMF. The reaction mixture was stirred for 1 hr and concentrated in vacuo. The residue (crude acyl chloride) was diluted with CH2Cl2 (10 mL) and pivalohydrazide (128 mg, 1.10 mmol) and triethylamine (0.31 mL, 2.21 mmol) was added. The reaction mixture was stirred for 2 hrs at room temperature. The reaction mixture was concentrated in vacuo and diluted with EtOAc (50 mL). The organic layer was washed with aq. 1N HCl and aq. sat'd NaHCO3 solution, dried over anhydrous MgSO4, filtered, and concentrated in vacuo. Purification by Prep-LC (Gilson) provided 244 mg (61%) of desired diamide as solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875647B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-55edbabeaad54a1ab3564d665f61bf4d
출처 메모uspto-grants-2011_01