참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Formylbenzoic acid | HCID 12088 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | Tert-butyl 3-aminopropanoate hydrochloride | HCID 16218890 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-[(2-tert-Butoxycarbonylethylamino)methyl]benzoic acid | HCID 59687909 | — |
반응 단계
Tert-butyl 3-aminopropanoate hydrochloride (5 g, 27.7 mmol) was dissolved in methanol (150 mL). Diisopropylethylamin (4.73 mL, 27.7 mmol) was added followed by 4-carboxybenzaldehyd. The mixture is heated to reflux for 1 hour. After cooling to room temperature sodium cyanoborohydride (1.77 g, 22.1 mmol) was added under nitrogen and stirred for 1 hour at room temperature. Acetic acid (15 mL) was added and the mixture was stirred for an additional 1 hour. The mixture was poured into water (300 mL) and stirred at room temperature over night. The water solution was washed with ethyl acetate (3×250 mL). The organic phase dried (Na2SO4) and solvent removed in vacuo to yield the crude product as an oil which solidifies by standing. The crude product was used in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08476228B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-529bb2850dd94b4484bee76555c5f515 |
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| 출처 메모 | uspto-grants-2013_07 |
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