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HRID 69560생성일: 2026년 10월 23일

Iodoacetic Acid → {2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid

https://huagongshe.com/ko/reaction/69560

반응식

참여 물질

역할이름HCID투입량
반응물Iodoacetic AcidHCID 5240—
반응물Sodium hydrideHCID 24758—
반응물Tert-butyl [5-(methoxymethyl)-1,3,4-thiadiazol-2-yl]carbamateHCID 84382575—
용매TetrahydrofuranHCID 8028—
생성물{2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acidHCID 6711689289.8%

반응 조건

온도60 °C

반응 단계

Iodoacetic acid (409.3 g, 2.2 mol, 1.5 eq) is added in one portion to a solution of tert-butyl [5-(methoxymethyl)-1,3,4-thiadiazol-2-yl]carbamate a31 (360 g, 1.468 mol, 1 eq) in tetrahydrofurane (3 l) at room temperature. Sodium hydride (52.83 g, 2.2 mol, 1.5 eq) is then added portionwise, in 30 minutes, at room temperature. The reaction mixture is heated at 60° C. for the night, and the solvent is evaporated under reduced pressure. Water is added to the residue, the solution is acidified to pH=2 with aqueous 6N HCl, then extracted with CH2Cl2. The organic layer is washed with 10% aqueous Na2S2O3 (to remove the coloration of iodine) and evaporated to dryness to furnish 455.7 g of {2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid a33 which is used directly in the next step without any further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822508B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0f53db14562843d99ed393f961dd7ad2
출처 메모uspto-grants-2014_09