참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 3-(3,4,5-Trimethoxyphenyl)acrylic acid | HCID 7021 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 3',4',5'-Trimethoxycinnamyl alcohol | HCID 73924 | — |
반응 단계
3,4,5-Trimethoxycinnamic acid (1.5 g) was dissolved in THF (100 mL), triethylamine (0.64 mL) was added to the solution under ice cooling, and ethyl chlorocarbonate (0.44 mL) was then added dropwise thereto. After stirring the resultant mixture at room temperature for 1 hour, sodium borohydride (477 mg) was added to the mixture under ice cooling. After stirring the resultant mixture at room temperature for 1 hour, diluted hydrochloric acid was added to the reaction mixture to conduct extraction with chloroform. The resultant organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1) to obtain the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06552188B2 |
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| 출처 데이터셋 | uspto-grants-2003_04 |
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| ORD ID | ord-b1259147d3e147f487dc04a96e5576dc |
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| 출처 메모 | uspto-grants-2003_04 |
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