참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrabutylammonium Fluoride Trihydrate | HCID 11726816 | — |
| 반응물 | N-allyl-N-tert.-butylsulphonylmethyl-(R)-glycidic acid amide | HCID 56993841 | — |
| 반응물 | ammonium fluoride THF | HCID 69831023 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | HCID 18604777 | HCID 18604777 | — |
반응 단계
A solution of 197 mg (0.757 mmol) of N-allyl-N-tert.-butylsulphonylmethyl-(R)-glycidic acid amide in 1 ml of tetrahydrofuran is introduced at 0°, with the exclusion of moisture, into 8 ml of a tetra-n-butyl; ammonium fluoride/THF solution which has been prepared from 5.0 g of tetra-n-butylammonium fluoride trihydrate by dehydrating at 60° C./0.1 torr and making up to 20 ml with tetrahydrofuran. The reaction mixture is stirred for 2 hours at room temperature and then partitioned between methylene chloride and phosphate buffer solution (pH 8.0). The crude product obtained by drying over sodium sulphate and concentration by evaporation of the organic phase is chromatographed over preparative silica gel plates using hexane/ethyl acetate (1:3). the title compound is obtained in the form of colourless crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04614614 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-4aba25dbbd1344a8bc8c659123e7942c |
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| 출처 메모 | uspto-grants-1986_09 |
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