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Hydrochloric Acid → 2,2'-Bithiophene, 5-phenyl-

HRID 466914
ノート
印刷プレビュー

反応式

HRID 466914 の反応式
[Mg].Br[C:3]1[S:4][CH:5]=[CH:6][CH:7]=1.Br[C:9]1[S:13][C:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:11][CH:10]=1.Cl>CCOCC.[Ni](Cl)Cl.C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[C:14]1([C:12]2[S:13][C:9]([C:3]3[S:4][CH:5]=[CH:6][CH:7]=3)=[CH:10][CH:11]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 138512-BromothiopheneHCID 27763132-Bromo-5-phenylthiopheneHCID 5462224Magnesium

生成物 1

HCID 4547572,2'-Bithiophene, 5-phenyl-収率 69.4%

試薬・触媒・溶媒 2

HCID 2724937
Dichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickel
触媒
HCID 3283Diethyl Ether溶媒3 回

実験手順

In 140 ml of ether, 17.4 g (0.725 mol) of magnesium shavings was reacted according to Grignard with 118 g (0.723 mol) of 2-bromothiophene, and this solution was then introduced into 280 ml of ether, 1.5 g (2.8 mmol) of 1,3-bis(diphenylphosphino)propane nickel dichloride and 140 g (0.586 mol) of 5-bromo-2-phenylthiophene. After the slightly exothermic reaction had subsided, the mixture was stirred for 4 hours at boiling point, and the solution thus obtained was then diluted with 280 ml of ether and stirred into 280 ml of 2N hydrochloric acid solution. The crystals which precipitated out were isolated and dried. There was obtained 98.4 g (69.4% of theory) of 5-phenyl-[2,2'-bithienyl], mp. 116.5°-118° C.

後処理

  1. customAfter the slightly exothermic reaction
  2. customthe solution thus obtained
  3. customThe crystals which precipitated out
  4. customwere isolated
  5. customdried

出典と根拠

ORDレコード
ord-c5032b8eae244781a9d4143b3c8a6f8c
出典データセット
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05158598

反応ノート

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