참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | CID 406 | HCID 406 | — |
| 반응물 | Dimethyl methylphosphonate | HCID 12958 | — |
| 반응물 | Cyclohexaneacetic acid, methyl ester | HCID 139743 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | Dimethyl (3-cyclohexyl-2-oxopropyl)phosphonate | HCID 14302183 | — |
반응 단계
A solution of 49.6 g (0.40 mole) dimethyl methylphosphonate (Aldrich) in 500 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 188 ml of 2.34 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 40 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 31.2 g (0.20 mole) methylcyclohexylacetate was added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 1.0 hour at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 25 ml acetic acid and rotary evaporated to a white gel. The gelatenous material was taken up in 75 ml water, the aqueous phase extracted with 100 ml portions of chloroform (3x), the combined organic extracts were backwashed (50 cc H 2 O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 160°-162° (0.2 mm) to give dimethyl 2-oxo-3-cyclohexylpropylphosphonate (2h).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04152527 |
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| 출처 데이터셋 | uspto-grants-1979_05 |
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| ORD ID | ord-d805ae2a3b1d4b668f257981756fa8e8 |
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| 출처 메모 | uspto-grants-1979_05 |
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