Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Allyl bromide → Methyl 2-allyloxy-5-methoxybenzoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Allyl bromide | HCID 7841 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | (S)-2,2,2-trifluoro-N-(6-methoxy-3-oxo-2,3-dihydro-1H-inden-1-yl)acetamide | HCID 1472787 | — |
| 반응물 | Methyl 2-hydroxy-5-methoxybenzoate | HCID 4072341 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | Methyl 2-allyloxy-5-methoxybenzoate | HCID 59560455 | 100% |
반응 단계
Step AS (1). A mixture of 10 g (55 mmol) of methyl 5-methoxysalicylate, 9.3 mL (110 mMol) of allyl bromide and 36 g (110 mmol) of cesium carbonate in 100 mL of acetonitrile was stirred at rt for 2 h. The reaction was filtered to remove cesium carbonate and concentrated under vacuum to yield 13.3 g (100%) of methyl 2-allyloxy-5-methoxybenzoate as a yellowish solid, which was used directly in the next reaction without purification. LC-MS (M+H)+=223; 1H NMR (400 MHz, CDCl3) δ ppm 3.77 (s, 3H) 3.88 (s, 3H) 4.49-4.58 (m, 2H) 5.20-5.29 (m, 1H) 5.39-5.50 (m, 1H) 5.96-6.11 (m, 1H) 6.89 (d, J=9.06 Hz, 1H) 6.98 (dd, J=9.07, 3.27 Hz, 1H) 7.32 (d, J=3.02 Hz, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07772221B2 |
| 출처 데이터셋 | uspto-grants-2010_08 |
| ORD ID | ord-fd18380c1d674437ad5ac44a1a8269e4 |
| 출처 메모 | uspto-grants-2010_08 |