Dichloromethane → HCID 131716472、化合物

HRID 2166002

反応式

HRID 2166002 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])C(Cl)=O.[OH:24][C:25]1[CH:30]=[CH:29][C:28](C2C=CC(C(OC[C@@H](C)CC)=O)=CC=2)=[CH:27][CH:26]=1.C(Cl)Cl.[C:48](OCC)(=[O:50])C>N1C=CC=CC=1>[F:1][C:2]1[C:10]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[C:9]([CH:8]=[CH:4][CH:3]=1)[C:48]([O:24][C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1)=[O:50]

参加物

6

実験手順

3-Fluoro-4-dodecyloxybenzoic acid chloride (3.32 g: 10 mmols) and 2.84 g (10 mmols) of (S)-2-methylbutyl 4'-hydroxybiphenyl-4-carboxylate were reacted in 10 ml of pyridine and 15 ml of methylene chloride for 3 hours under reflux. After the reaction mixture was left to cool, 50 ml of ethyl acetate was added, and washed twice with 10% hydrochloric acid and once with each of a saturated sodium bicarbonate aqueous solution, water and a saturated sodium chloride aqueous solution. After the reaction product was dried with anhydrous sodium sulfate, the solvent was concentrated. Crude crystals obtained were purified by silica gel column chromatography (solvent: chloroform-hexane), and recrystallized from ethanol to obtain 4.64 g of 4{(S)-2-methylbutyloxycarbonyl]phenyl)phenyl 3-fluoro-dodecyloxybenzoate.

後処理

  1. waitAfter the reaction mixture was left
  2. temperatureto cool
  3. washwashed twice with 10% hydrochloric acid
  4. dry with materialAfter the reaction product was dried with anhydrous sodium sulfate
  5. concentrationthe solvent was concentrated
  6. customCrude crystals obtained
  7. customwere purified by silica gel column chromatography (solvent: chloroform-hexane)
  8. customrecrystallized from ethanol

出典と根拠

ORDレコード
ord-8fd63501fdbe4a128189ddda3b992b1f
出典データセット
uspto-grants-1990_07
特許番号
US04943386

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