Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1172825생성일: 2026년 10월 26일
Hexane → [4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanol
https://huagongshe.com/reaction/1172825
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | (2-Chloro-6-fluoro-3-methoxyphenyl)trimethylsilane | HCID 46941339 | — |
| 반응물 | 4-(4-Chlorophenoxy)-2-propylbenzaldehyde | HCID 57420143 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanol | HCID 86622409 | — |
반응 단계
To a solution of 2,2,6,6-tetramethylpiperidine (2.75 g, 10 mmol) in THF (50 mL) cooled at −75° C. was added a solution of n-butyllithium in hexane (1.6 M, 6.3 mL, 10 mmol). After 15 min, 4-fluoro-2-chloro-3-(trimethylsilyl)anisole (2.3 g, 10 mmol) was added and the solution was warmed gradually to −40° C. over a 2 h period. The solution was recooled to −75° C. and a solution of the aldehyde from Step 1 of Example 3 (1.4 g, 5.0 mmol) in THF (3 mL) was added quickly. The reaction mixture was stirred for 15 min., poured into a saturated aqueous solution of ammonium chloride and extracted with ethyl acetate. After removal of the solvent, the residue was purified by chromatography on silica gel to give the title product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07834036B2 |
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| 출처 데이터셋 | uspto-grants-2010_11 |
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| ORD ID | ord-8ab7dbe4dfac470a9b7aa4d9fdbe6be1 |
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| 출처 메모 | uspto-grants-2010_11 |
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