Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1851714생성일: 2026년 10월 27일
Iodoacetic Acid → {2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid
https://huagongshe.com/reaction/1851714
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodoacetic Acid | HCID 5240 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Tert-butyl [5-(methoxymethyl)-1,3,4-thiadiazol-2-yl]carbamate | HCID 84382575 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | {2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid | HCID 67116892 | 90% |
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 a13 (360 g, 1.47 mol, 1 eq) in tetrahydrofurane (3 l) at room temperature. Sodium hydride (52.8 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. overnight, 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 sodium thiosulfate and evaporated to dryness to afford 455.7 g of {2-[(tert-butoxy-carbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid a14 which is used directly in the next step without any further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08957218B2 |
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| 출처 데이터셋 | uspto-grants-2015_02 |
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| ORD ID | ord-a5c89827bc5643c2a4dbdcb84fa5fb1c |
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| 출처 메모 | uspto-grants-2015_02 |
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