戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 42793作成日:2026年10月26日

Nitrogen → [4-(Chloromethyl)-1,3-thiazol-2-yl]methanol

https://huagongshe.com/reaction/42793

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Potassium Sodium TartrateHCID 9357—
反応物Diisobutylaluminum hydrideHCID 14487—
反応物Ethyl 4-(chloromethyl)-1,3-thiazole-2-carboxylateHCID 10822129—
溶媒TetrahydrofuranHCID 8028—
生成物[4-(Chloromethyl)-1,3-thiazol-2-yl]methanolHCID 11073749—

反応条件

温度-78 °C

反応手順

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-chloromethyl-thiazole-2-carboxylic acid ethyl ester (2.47 g, 12.03 mmol) in THF (120.0 mL) was treated at −78° C. with DiBAL (36.09 mL of a 1M sol in THF, 36.09 mmol) and the reaction mixture was stirred for 1 h at −78° C. and the allowed to warm to rt over 1 h. The reaction mixture was poured over a sat. aq. Rochelle's salt sol. and stirred for 1 h at rt. The aq. layer was extracted with EtOAc (2×150 mL) and the combined org. layer was washed with brine (200 mL). The organic layer was dried over MgSO4, filtered, and the solvent removed under reduced pressure. Purification of the residue by FC (1:1 hept-EA) gave the title compound as a light yellow oil. TLC:rf (1:1 hept-EA)=0.30. LC-MS-conditions 02: tR=0.59 min, [M+H]+=164.07.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536209B2
出典データセットuspto-grants-2013_09
ORD IDord-39cb831c15c84561a45ac6c7c947f6fb
出典メモuspto-grants-2013_09