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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14562생성일: 2026년 10월 24일

2-Butyn-1-ol → 4-(2-Butynyloxy)-6-chloropyrimidine

https://huagongshe.com/ko/reaction/14562

반응식

참여 물질

역할이름HCID투입량
반응물2-Butyn-1-olHCID 12991—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물4,6-DichloropyrimidineHCID 70943—
용매TetrahydrofuranHCID 8028—
생성물4-(2-Butynyloxy)-6-chloropyrimidineHCID 1213760285.9%

반응 단계

1.05 g of sodium hydride (60% oil suspension) was suspended in 24 ml of tetrahydrofuran. 8 ml of tetrahydrofuran solution of 1.42 g of 2-butyn-1-ol was added dropwise at room temperature therein slowly, and the mixture was stirred for 20 minutes. Into the mixture was added dropwise 8 ml of tetrahydrofuran solution of 3 g of 4,6-dichloropyrimidine at 0° C. slowly, and stirred for 4 hours. The reaction mixture was poured into a saturated ammonium chloride aqueous solution, and the mixture was extracted with chloroform three times. The organic layers were washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 3.16 g of 4-chloro-6-(2-butynyloxy) pyrimidine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732448B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-cf9f3e4130dd49c5864e4fef290d66b4
출처 메모uspto-grants-2010_06