참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl orthoformate | HCID 31214 | — |
| 반응물 | Neopentyl glycol | HCID 31344 | — |
| 반응물 | 6-Bromo-2-hydroxy-3-methoxybenzaldehyde | HCID 262237 | — |
| 촉매 | p-Toluenesulfonic acid | HCID 6101 | — |
| 생성물 | 3-Bromo-2-(5,5-dimethyl-[1,3]dioxan-2-yl)-6-methoxy-phenol | HCID 59761836 | 100% |
반응 단계
A mixture of 6-bromo-2-hydroxy-3-methoxy-benzaldehyde (2.31 g, 10.0 mmol), neopentyl glycol (1.14 g, 11.0 mmol), TsOH (9.5 mg) and triethyl orthoformate (1.93 g, 13.0 mmol) were heated at 110° C. for 30 min and then partitioned between NaHCO3 (300 mL) solution and EtOAc (200 mL). The aqueous layer was extracted with EtOAc (3×30 mL) and the combined extracts were washed with brine and dried through Na2SO4. Evaporation of solvent afforded the title compound (3.17 g, 100%). 1H NMR (CDCl3) δ 0.85 (s, 3H), 1.27 (s, 3H), 3.70 (s, 2H), 3.82 (s, 2H), 3.85 (s, 3H), 5.90 (s, 1H), 6.72 (d, J=8 Hz, 1H), 7.02 (d, J=8 Hz, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09290503B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-c1ede8de17c641598a8aca29cbf778de |
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| 출처 메모 | uspto-grants-2016_03 |
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