反応 #833520

ord-1a7d2ccaa30d43bcb5ba1e4ede0c0490

反応方程式

COc1ccc(OC)cc1
1,4-dimethoxybenzene
CCCCCCCCCCOc1ccc(-c2ccc(OCCCCCCCCCC)c(OCCCCCCCCCC)c2)cc1OCCCCCCCCCC
Solid 3a
CCCCCCCCCCOc1ccc(-c2ccc(OCCCCCCCCCC)c(OCCCCCCCCCC)c2)cc1OCCCCCCCCCC
3,3′,4,4′-tetrakisdecyloxybiphenyl
CCCCCCCCCCOc1cc2c3cc(OCCCCCCCCCC)c(OCCCCCCCCCC)cc3c3c(OC)ccc(OC)c3c2cc1OCCCCCCCCCC
4a
収率 84.0%
CCCCCCCCCCOc1cc2c3cc(OCCCCCCCCCC)c(OCCCCCCCCCC)cc3c3c(OC)ccc(OC)c3c2cc1OCCCCCCCCCC
1,4-dimethoxy-6,7,10,11-tetrakis(decyloxy)triphenylene
収率 84.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The reaction mixture was quenched with anhydrous MeOH (30 mL)
  2. 2
    workup.ADDITIONwas added to the resulting oil
  3. 3
    洗浄washed with MeOH
  4. 4
    その他The product was further purified by column chromatography

実験手順

Solid 3a (5.50 g, 7.06 mmol) was added to an ice cold suspension of anhydrous FeCl3 (9.16 g, 56.5 mmol) in dry CH2Cl2 (250 mL). Within 2 min 1,4-dimethoxybenzene (3.90 g, 28.2 mmol) was added to the green reaction mixture. The reaction mixture was allowed to warm slowly to room temperature and then stir for an additional 12 h. The reaction mixture was quenched with anhydrous MeOH (30 mL). The volume of the mixture was reduced to 50 mL under reduced pressure and MeOH (200 mL) was added to the resulting oil. The slightly violet product was called on a frit and washed with MeOH. The product was further purified by column chromatography using a 50% CH2Cl2/50% hexane solvent mixture to afford 4a (RF=0.24) as a colorless solid in 84% yield (mp 69-70° C.).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07393503B2uspto-grants-2008_07