참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Lithiumtriethylborohydride | HCID 23664628 | — |
| 반응물 | tert-Butyl (S)-2-(((methylsulfonyl)oxy)methyl)azetidine-1-carboxylate | HCID 59371380 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (R)-Tert-butyl 2-methylazetidine-1-carboxylate | HCID 57784717 | 30% |
반응 단계
2-(S)-Methanesulfonyloxymethyl-azetidine-1-carboxylic acid tert-butyl ester was (4.83 g, 18.2 mmol) was taken up in THF (11 mL), cooled to 0° C. under N2, treated drop-wise with a lithium triethylborohydride (1.0 M in THF, 73 mL), stirred at ambient temperature for 6 hours, treated with ethyl acetate (500 mL), washed with water, washed with 0.25 M HCl, washed with NaHCO3 solution, washed with brine (2×), dried (MgSO4), filtered, concentrated and purified by chromatography on silica gel eluting with a gradient of 10:1 and then 5:1 hexane:ethyl acetate to provide 0.95 g (30%) of the title compound. 1H NMR (300 MHz, CDCl3) δ 1.37 (d, J=6.10 Hz, 3 H) 1.44 (s, 9 H) 1.76 (m, 1 H) 2.27 (m, 1 H) 3.81 (t, J=7.46 Hz, 2 H) 4.28 (m, 1 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07094790B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-98a2701b80cf40f4b520ee3818c90065 |
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| 출처 메모 | uspto-grants-2006_08 |
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