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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexamethylphosphoramide | HCID 12679 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Tetrahydro-2-(2-propynyloxy)-2H-pyran | HCID 98609 | — |
| 반응물 | 2-(2-Bromoethyl)cyclopropylmethyl t-butyldimethyl silyl ether | HCID 21760427 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(5-Tetrahydropyranyloxy-3-pentynyl)cyclopropylmethyl t-butyldimethylsilyl ether | HCID 54030042 | 82.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05416231 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-95a8518022b348ec9a34488da3a803fd |
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| 출처 메모 | uspto-grants-1995_05 |
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