참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromoform | HCID 5558 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | 4-Isopropoxybenzaldehyde | HCID 250077 | — |
| 반응물 | Potassium hydroxide methanol | HCID 23689386 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2-(4-Isopropoxyphenyl)-2-methoxyacetic acid | HCID 58432042 | — |
반응 단계
An oven-dried flask was charged with 4-isopropoxybenzaldehyde (4.9 g, 29.9 mmol), anhydrous methanol (30 mL) and anhydrous dioxane (30 mL) then fitted with an addition funnel. The addition funnel was charged with a solution of KOH (8.4 g, 149.5 mmol) in anhydrous methanol (30 mL) and an aliquot (˜2 mL) was added to the reaction mixture. Bromoform (3.4 mL, 38.8 mmol) was added to the reaction mixture then the remaining KOH/MeOH solution was added dropwise over 10 minutes. After stirring for 18 hours, the mixture was concentrated in vacuo. The residue was diluted with water and the pH was adjusted to ˜2 using concentrated HCl then extracted with EtOAc. The combined organics were dried over Na2SO4 and filtered. Concentration of the filtrate in vacuo gave 2-(4-isopropoxyphenyl)-2-methoxyacetic acid as a light yellow solid (6.8 g) which was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434707B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-e9c5eccb47884e1e8730c24ca8b655c2 |
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| 출처 메모 | uspto-grants-2016_09 |
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