戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 517799作成日:2026年10月26日

Water → Phenyl(6-thiocyanato-1,3-benzothiazol-2-yl)carbamate

https://huagongshe.com/reaction/517799

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Phenyl chloroformateHCID 15891—
反応物2-Amino-6-thiocyanato-1,3-benzothiazoleHCID 81600—
反応物Sodium BicarbonateHCID 516892—
溶媒TetrahydrofuranHCID 8028—
生成物Phenyl(6-thiocyanato-1,3-benzothiazol-2-yl)carbamateHCID 5347257087.4%

反応条件

温度20 °C

反応手順

7.5 g of phenyl chlorocarbonate and then 4.05 g of sodium hydrogen carbonate and 9.4 cm3 of water are added, at 20° C., to a solution of 2.5 g of commercial 2-amino-1,3-benzothiazol-6-yl thiocyanate in 94 cm3 of tetrahydrofuran. The resulting mixture is subsequently stirred at 20° C. for 20 h and then extracted with 2×150 cm3 of ethyl acetate. The organic phases are combined and then washed with 3×50 cm3 of a saturated aqueous solution of sodium hydrogen carbonate. The organic phase obtained is dried over magnesium sulphate and then concentrated to dryness under reduced pressure. The residue is taken up in 50 cm3 of water and the product is spin-filter-dried and dried under vacuum at 20° C. 3.45 g of phenyl (6-thiocyanato-1,3-benzothiazol-2-yl)carbamate are thus obtained in the form of a pale yellow solid, the characteristics of which are as follows:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115134B2
出典データセットuspto-grants-2015_08
ORD IDord-789fd4d4ec1a4d488f529b42e8d9665e
出典メモuspto-grants-2015_08