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Triphenylphosphine → HCID 68408307、化合物

HRID 1176163
ノート
印刷プレビュー

反応式

HRID 1176163 の反応式
[CH2:1]([O:13][C:14]1[CH:19]=[CH:18][C:17](I)=[CH:16][CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:40][Si:41]([C:44]#[CH:45])([CH3:43])[CH3:42].[NH4+].[Cl-]>N1CCCCC1.[Cu]I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[CH2:1]([O:13][C:14]1[CH:19]=[CH:18][C:17]([C:45]#[C:44][Si:41]([CH3:43])([CH3:42])[CH3:40])=[CH:16][CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 11776TriphenylphosphineHCID 25517Ammonium ChlorideHCID 66111TrimethylsilylacetyleneHCID 10883601Benzene, 1-(dodecyloxy)-4-iodo-

生成物 1

HCID 68408307HCID 68408307、化合物

試薬・触媒・溶媒 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
触媒
HCID 178418476HCID 178418476、化合物触媒
HCID 8082Piperidine溶媒

反応条件

温度
50 °C

実験手順

4-(Dodecyloxy)iodobenzene (4.04 g, 1.04×10−2 mol), triphenylphosphine (0.165 g, 6.29×10−4 mol), CuI (0.108 g, 5.67×10−4 mol) and Pd(PPh3)2Cl2 (0.153 g, 2.18×10−4 mol) were dissolved in 40 ml of dry piperidine under N2. (Trimethylsilyl)acetylene (3.00 ml, 2.12×10−2 mol) was added and the mixture was stirred at 50° C. for 6 h under N2. After cooling, the reaction mixture was poured into aq. NH4Cl and extracted with CH2Cl2 (three times). The combined organic layers were washed with aq. NH4Cl, water, and dried over Na2SO4. The crude product was chromatographed on silica gel with 4:1 hexane:CH2Cl2 as the eluent. Yield=3.633 g (97% based on 4.04 g of 4-(dodecyloxy)iodobenzene). 1H NMR (250 MHz, CDCl3): δ 7.39 (d, 2H, J=8.9 Hz, Ph), 6.80 (d, 2H, J=9.0 Hz, Ph), 3.94 (t, 2H, J=6.6 Hz, —OCH2—), 1.77 (quint, 2H, J=6.6 Hz, —OCH2CH2—), 1.17-1.50 (m, 18H, —CH2—), 0.88 (t, 3H, J=6.6 Hz, —CH3), 0.24 (s, 9H, Si—CH3). CI MS m/z: 358.268 (M+) (calcd 358.269).

後処理

  1. temperatureAfter cooling
  2. extractionextracted with CH2Cl2 (three times)
  3. washThe combined organic layers were washed with aq. NH4Cl, water
  4. dry with materialdried over Na2SO4
  5. customThe crude product was chromatographed on silica gel with 4:1 hexane

出典と根拠

ORDレコード
ord-06155a86bd304016abeaf05e10819f05
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07842758B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート