Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132621생성일: 2026년 10월 23일
(S)-4-methylbenzenesulfinamide → 4-Methyl-benzenesulfinic Acid ((2R,3R)-2,3-dimethyl-hexylidene)-amide
https://huagongshe.com/ko/reaction/132621
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (S)-4-methylbenzenesulfinamide | HCID 11116285 | — |
| 반응물 | (2R,3R)-2,3-Dimethyl-hexanal | HCID 57444839 | — |
| 촉매 | Titanium tetraethoxide | HCID 76524 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Sodium chloride; water | HCID 57417360 | — |
| 생성물 | 4-Methyl-benzenesulfinic Acid ((2R,3R)-2,3-dimethyl-hexylidene)-amide | HCID 86597955 | 51.7% |
반응 단계
Titanium(IV) ethoxide (5.16 g, 22.6 mmol) and (S)-(+)-p-toluenesulfinamide (7.02 g, 45.2 mmol) were added to (2R,3R)-2,3-dimethyl-hexanal (2.9 g, 22.6 mmol) in dry THF (30 mL). The resulting mixture was stirred at room temperature for 18 hours and poured into a brine solution (40 mL). The slurry was rapidly stirred for 10 minutes and filtered. The filtrate was extracted into ethyl acetate, washed with brine and dried over MgSO4. The solvent was evaporated and the residue was filtered through a silica plug, eluting with 50/50 solution of hexane/ethyl acetate to afford the titled compound (3.1 g, 51.6% yield) as an oil: 1H NMR (400 MHz, CDCl3) δ ppm 0.8 (m, 6H) 1.1 (m, 4H) 1.3 (m, 3H) 1.7 (m, 1H) 2.4 (s, 3H) 2.5 (m, 1H) 7.3 (d, J=8.3 Hz, 2H) 7.5 (d, J=8.1 Hz, 2H) 8.1 (d, J=5.4 Hz, 1H). MS, m/z (relative intensity): 266 [M+1H, 100%].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07388023B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-4e901b5c056e4996a8548ae3e5c5700d |
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| 출처 메모 | uspto-grants-2008_06 |
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