참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 2-Octyldodecanol | HCID 21414 | — |
| 반응물 | 5,10-Dimethoxynaphtho[2,3-b:6,7-b']dithiophene | HCID 68359379 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5,10-Bis(2-octyldodecyloxy)naphtho[2,3-b:6,7-b']dithiophene | HCID 70873007 | 66% |
반응 단계
Compound (3) (0.400 g, 1.33 mmol) was weighed into a flame-dried 2-neck flask fitted with a condenser. Toluene (13 mL), 2-octyl-1-dodecanol (1.59 g, 5.32 mmol), and p-toluenesulfonic acid (0.051 g, 0.266 mmol) were then added. The mixture was placed in a 130° C. heat bath and stirred overnight. The mixture was diluted with water, extracted with dichloromethane, dried over MgSO4, filtered and concentrated. The product was purified via column chromatography (10% dichloromethane in hexanes) to yield compound (4a) as a yellow solid (0.735 g, 66%). 1H NMR (500 MHz, CDCl3, 298 K): 8.46 (s, 2H); 7.45 (m, 4H); 4.27 (d, J=5.4 Hz, 4H); 2.01 (quintet, J=6.2 Hz, 2H); 1.73 (m, 4H); 1.47 (m, 60H); 0.89 (m, 12H) ppm. 13C NMR (125 MHz, CDCl3, 298 K): 149.87; 139.70; 127.98; 127.08; 124.83; 124.62; 110.84; 75.85; 39.38; 31.96; 31.42; 30.18; 29.76; 29.71; 29.43; 29.41; 27.06; 22.74; 14.18 ppm. HRMS (ESI-TOF-MS): m/z calcd for C54H88O2S2 832.6220, found 832.6217.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08754188B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-cc38b86ca2dc4fa0b5b0707960462229 |
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| 출처 메모 | uspto-grants-2014_06 |
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