참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 1,3-Dithiane | HCID 10451 | — |
| 반응물 | 5-Bromo-1-indanone | HCID 520695 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-bromo-1-(1,3-dithian-2-yl)-2,3-dihydro-1H-inden-1-ol | HCID 57419484 | 71.2% |
반응 단계
To a solution of 1,3-dithiane (1.82 g, 14.7 mmol) in dry THF (20 ml) was added n-butyllithium (8.62 ml, 13.8 mmol, 1.6 M in hexane) dropwise at −30° C. The resulting mixture was stirred for 2 h at −15° C. Then, a solution of 5-bromo-2,3-dihydro-1H-inden-1-one (2 g, 9.19 mmol) in dry THF (24 ml) was added dropwise, maintaining the temperature between −15° C. and −6° C. After the addition was completed, the brown solution was allowed to warm to 0° C. and was then stored in the fridge overnight. Then, 1N HCl was added and the brown mixture was extracted two times with diethylether. The combined organic layers were washed with brine, dried with Na2SO4 and evaporated. The remaining residue was purified by chromatography (silica gel; heptane/EtOAc 90:10-75:25) to obtain the title compound as light yellow gum (2.167 g, 71%). MS: 330.1 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08592426B2 |
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| 출처 데이터셋 | uspto-grants-2013_11 |
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| ORD ID | ord-2267c5a4830640a0830f5cba6c1dc3d5 |
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| 출처 메모 | uspto-grants-2013_11 |
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