Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → 4-Bromo-2-(hydroxymethyl)-6-methoxyphenol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | 5-Bromo-2-hydroxy-3-methoxybenzaldehyde | HCID 262238 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Bromo-2-(hydroxymethyl)-6-methoxyphenol | HCID 894092 | 99.1% |
반응 단계
To a 200 ml solution of 50 g of 5-bromo-2-hydroxy-3-methoxybenzaldehyde in an ethanol:THF=1:1 mixed solvent there was added 16.4 g of sodium borohydride while cooling on ice. After stirring for 2 hours at room temperature, 1N hydrochloric acid was added to the reaction mixture while cooling on ice. The organic layer was extracted with ethyl acetate and dried over anhydrous magnesium sulfate. The desiccant was filtered out and the filtrate was concentrated under reduced pressure to obtain the target compound (50 g) as a crude product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07807690B2 |
| 출처 데이터셋 | uspto-grants-2010_10 |
| ORD ID | ord-06294e2154934eb6b935b5e72e55bad4 |
| 출처 메모 | uspto-grants-2010_10 |