戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 69560作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Iodoacetic AcidHCID 5240—
反応物Sodium hydrideHCID 24758—
反応物Tert-butyl [5-(methoxymethyl)-1,3,4-thiadiazol-2-yl]carbamateHCID 84382575—
溶媒TetrahydrofuranHCID 8028—
生成物{2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acidHCID 6711689289.8%

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822508B2
出典データセットuspto-grants-2014_09
ORD IDord-0f53db14562843d99ed393f961dd7ad2
出典メモuspto-grants-2014_09