참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 4-Hydroxyphenylboronic acid | HCID 2734360 | — |
| 반응물 | 3,4-Dibromothiophene-2-carbaldehyde | HCID 12559528 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Ethanol toluene water | HCID 86587398 | — |
| 생성물 | 4-Bromo-3-(4-hydroxyphenyl)thiophene-2-carbaldehyde | HCID 86671493 | 17% |
반응 단계
A mixture of 3,4-dibromothiophene-2-carbaldehyde (see Intermediate 1 (see Example 15 for Intermediate synthesis)) (2.0 g, 7.5 mmol), 4-hydroxyphenylboronic acid (Scheme II, 8A, X1=4-hydroxyphenyl) (1.0 g, 7.5 mmol), Na2CO3 (1.6 g, 15 mmol), and Pd(PPh3)4 (431 mg, 0.37 mmol) in toluene/EtOH/H2O (30 mL, 5:3:2) was heated to 80° C. and stirred overnight under nitrogen. When TLC indicated that the starting material was consumed, the mixture was diluted with water, neutralized to pH=4-5 with HCl (1M), extracted with EtOAc, concentrated, and purified by column chromatography (PE:EtOAc=20:1) to give 4-bromo-3-(4-hydroxyphenyl)thiophene-2-carbaldehyde (Scheme II, 8, X1=4-hydroxyphenyl) (350 mg, yield 17%) as a white solid. 1H NMR (DMSO-d6 400 MHz): δ9.90 (s, 1H), 9.53 (s, 1H), 8.33 (s, 1H), 7.33 (d, J=8.4 Hz, 2H), 6.91 (d, J=8.4 Hz, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08859611B2 |
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| 출처 데이터셋 | uspto-grants-2014_10 |
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| ORD ID | ord-921792d5865d4682be7401a285764e34 |
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| 출처 메모 | uspto-grants-2014_10 |
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