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Triethylamine → 1H-Inden-2-yl(diisopropyl)phosphine

HRID 1350349
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HRID 1350349 반응식
Br[C:2]1[CH2:3][C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2.[PH:11]([CH:15]([CH3:17])[CH3:16])[CH:12]([CH3:14])[CH3:13].CCN(CC)CC>C1(C)C=CC=CC=1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH:10]=[C:2]1[P:11]([CH:15]([CH3:17])[CH3:16])[CH:12]([CH3:14])[CH3:13]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 536496Di-i-propylphosphineHCID 5755861H-Indene, 2-bromo-

생성물 1

HCID 210959941H-Inden-2-yl(diisopropyl)phosphine

시약·촉매·용매 2

HCID 178418397HCID 178418397, 화합물촉매HCID 1140Toluene용매

실험 절차

Following the procedure described for the synthesis of 3 (method A), 15.81 g (0.081 mol) of 2-bromo-1H-indene, 9.54 g (0.081 mol) of iPr2PH, 13.9 ml (10.09 g, 0.100 mol) of Et3N, and 2.95 g (2.55 mmol) of Pd(PPh3)4 in 60 ml of toluene gave 1H-Inden-2-yl(diisopropyl)phosphine. The crude product was distilled in vacuum (104–106° C./2 mm). Yield 14.8 g (80%) of colorless oil of 1H-Inden-2-yl(diisopropyl)phosphine, 4.

출처 및 근거

ORD 기록
ord-24fdcc1a2f75492a98c1cb7e1a634bd3
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07214747B2

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