참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | (Formyloxy)acetonitrile | HCID 4205685 | — |
| 반응물 | (2-Amino-5-methoxyphenyl)methanol | HCID 13756678 | — |
| 생성물 | Formic acid (2-formylamino-5-methoxybenzyl)ester | HCID 86596179 | — |
반응 단계
A solution of 7.00 g of (2-amino-5-methoxyphenyl)methanol, 9.8 ml of formic acid cyanomethyl ester and 0.05 g of 4-N,N-(dimethylamino)pyridine in 30 ml of anhydrous tetrahydrofuran was heated for 5 hours under reflux. The solution was then concentrated by evaporation in vacuo and the residue was taken up in 100 ml of ethyl acetate. Crystals formed on cooling the solution to 0° C., which were suction filtered, washed with methanol, and dried in vacuo. 7.20 g (75% of theory) of the title compound were thereby obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07183274B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-277ff5e3f8794036a77bcf51628f651d |
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| 출처 메모 | uspto-grants-2007_02 |
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