참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dimethyl-3-nitrobenzene | HCID 6739 | — |
| 반응물 | Diethyl Oxalate | HCID 7268 | — |
| 반응물 | Potassium ethoxide | HCID 23670592 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2-(2-Methyl-6-nitrophenyl)acetic acid | HCID 675115 | 45% |
반응 단계
Diethyl oxalate (30 mL) in 20 mL of dry ether was added with stirring to 19 g of potassium ethoxide suspended in 50 mL of dry ether. The mixture was cooled in an ice bath and 20 mL of 3-nitro-o-xylene in 20 mL of dry ether was slowly added. The thick dark red mixture was heated to reflux for 0.5 hr, concentrated to a dark red solid, and treated with 10% sodium hydroxide until almost all of the solid dissolved. The dark red mixture was treated with 30% hydrogen peroxide until the red color changed to yellow. The mixture was treated alternately with 10% sodium hydroxide and 30% hydrogen peroxide until the dark red color was no longer present. The solid was filtered off and the filtrate acidified with 6N hydrochloric acid. The resulting precipitate was collected by vacuum filtration, washed with water, and dried under vacuum to give 9.8 g (45% yield) of 2-methyl-6-nitrophenylacetic acid as an off-white solid. The solid was hydrogenated in methanol over 10% palladium on carbon to give 9.04 g of the title compound as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06855730B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-6e4d00333b5f44c18b0da791bf3f2939 |
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| 출처 메모 | uspto-grants-2005_02 |
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