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Trimethylsilylacetylene → [4-(1-Methoxycyclopropyl)phenylethynyl]-trimethylsilane

HRID 278702
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HRID 278702 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]2([O:11][CH3:12])[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[CH3:13][Si:14]([C:17]#[CH:18])([CH3:16])[CH3:15]>C(N(CC)CC)C.O1CCCC1.[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>[CH3:12][O:11][C:8]1([C:5]2[CH:6]=[CH:7][C:2]([C:18]#[C:17][Si:14]([CH3:16])([CH3:15])[CH3:13])=[CH:3][CH:4]=2)[CH2:10][CH2:9]1
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참가 물질

7

반응물 2

HCID 66111TrimethylsilylacetyleneHCID 225689901-Bromo-4-(1-methoxycyclopropyl)benzene2회

생성물 1

HCID 22568890[4-(1-Methoxycyclopropyl)phenylethynyl]-trimethylsilane수율 90%

시약·촉매·용매 4

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 178418476
HCID 178418476, 화합물
촉매
HCID 8028Tetrahydrofuran용매
HCID 8471Triethylamine용매

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온도
70 °C

실험 절차

Using General Procedure D; 1-bromo-4-(1-methoxycyclopropyl)-benzene (Intermediate 59, 300.0 mg, 1.32 mmol) in triethylamine (4 mL) and anhydrous tetrahydrofuran (4 mL) was treated with copper(I)iodide (93.0 mg, 0.13 mmol) and then sparged with argon for 5 minutes. Trimethylsilyl acetylene (1.39 g, 14.2 mmols) was then added followed by dichlorobis(triphenylphosphine)palladium(II) (93.0 mg, 0.13 mmol). The resulting reaction mixture was heated to 70° C. for 60 h. The title compound (286.0 mg, 90%) was isolated by chromatography (0-3% EtOAc-hexanes).

후처리

  1. customsparged with argon for 5 minutes
  2. customThe resulting reaction mixture

출처 및 근거

ORD 기록
ord-dd88ea43e41c4555ba61d804e303b1e0
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06359135B1

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