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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393410생성일: 2026년 10월 24일

N-Boc-p-toluenesulfonamide → tert-Butyl methyl(tosyl)carbamate

https://huagongshe.com/ko/reaction/393410

반응식

참여 물질

역할이름HCID투입량
반응물N-Boc-p-toluenesulfonamideHCID 688170—
반응물Diethyl azodicarboxylateHCID 5462977—
용매MethanolHCID 887—
생성물tert-Butyl methyl(tosyl)carbamateHCID 2266006785%

반응 단계

The crude fluorous DEAD reagent 22 was then used in Mitsunobu reactions with N-Boc-p-toluenesulfonamide. Once again, the standard mode of addition gave complete conversion with MeOH and the product, N-methyl-N-boc-p-toluenesulfonamide was isolated in 85% yield after FSPE. However, the allyl alcohol gave only trace conversion of the starting material. The organic fraction after FSPE was mostly starting material. These results are summarized in Table 7.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06806357B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-41a99d97be5e482e8c5bb07a1cfdf604
출처 메모uspto-grants-2004_10