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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42793생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/42793

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Potassium Sodium TartrateHCID 9357—
반응물Diisobutylaluminum hydrideHCID 14487—
반응물Ethyl 4-(chloromethyl)-1,3-thiazole-2-carboxylateHCID 10822129—
용매TetrahydrofuranHCID 8028—
생성물[4-(Chloromethyl)-1,3-thiazol-2-yl]methanolHCID 11073749—

반응 조건

온도-78 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536209B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-39cb831c15c84561a45ac6c7c947f6fb
출처 메모uspto-grants-2013_09