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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36810생성일: 2026년 10월 24일

Hexamethylphosphoramide → 2-(5-Tetrahydropyranyloxy-3-pentynyl)cyclopropylmethyl t-butyldimethylsilyl ether

https://huagongshe.com/ko/reaction/36810

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물Ammonium ChlorideHCID 25517—
반응물Tetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
반응물2-(2-Bromoethyl)cyclopropylmethyl t-butyldimethyl silyl etherHCID 21760427—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-(5-Tetrahydropyranyloxy-3-pentynyl)cyclopropylmethyl t-butyldimethylsilyl etherHCID 5403004282.6%

반응 조건

온도0 °C

반응 단계

A tetrahydrofuran solution (15 ml) of propargyl alcohol tetrahydropyranyl ether (1.44 g, 10.3 mmol) was cooled to -78° C., and butyllithium (factor=1.5, 6.9 ml, 10.3 mmol) was added thereto. Fifteen minutes later, the temperature was raised to 0° C. Hexamethylphosphoric triamide (3.76 ml, 21 mmol) was added thereto, and the mixture was stirred for 15 minutes. A tetrahydrofuran solution of 2-(2-bromoethyl)cyclopropylmethyl t-butyldimethyl silyl ether (2.73 g, 10.3 mmol) was added thereto, and the mixture was stirred at room temperature for 2 hours. A saturated ammonium chloride solution was added thereto, and the product was extracted with ethyl ether. The crude product was purified by silica gel column chromatography to obtain 2-(5-tetrahydropyranyloxy-3-pentynyl)cyclopropylmethyl t-butyldimethylsilyl ether (3 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05416231
출처 데이터셋uspto-grants-1995_05
ORD IDord-95a8518022b348ec9a34488da3a803fd
출처 메모uspto-grants-1995_05