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1,1′-(1,4-Butanediyl)bis[1-phenylphosphine] → HCID 53960761, 화합물

HRID 1379917
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HRID 1379917 반응식
[CH3:1][C@@H:2]([CH2:6][CH2:7][CH:8](O)[C:9]([CH3:11])=[CH2:10])[CH2:3][CH2:4][OH:5].C1(PCCCCPC2C=CC=CC=2)C=CC=CC=1>[Pd](Cl)Cl.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:1][C@@H:2]([CH2:6][CH:7]=[CH:8][C:9]([CH3:11])=[CH2:10])[CH2:3][CH2:4][OH:5]
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참가 물질

4

반응물 2

HCID 166877121,1′-(1,4-Butanediyl)bis[1-phenylphosphine]HCID 86751364HCID 86751364, 화합물

생성물 1

HCID 53960761HCID 53960761, 화합물수율 82%

시약·촉매·용매 1

HCID 6102075Dichlorobis(triphenylphosphine)palladium촉매

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온도
150 °C

실험 절차

(S)-3,7-dimethyl-6-hydroxy-7-octene-1-ol (I) (10.0 g, 58.1 mmol), bis(triphenylphosphine) palladium chloride (40.8 mg, 0.058 mmol), and 1,4-bisphenylphosphinobutane (1.24 g, 2.91 mmol) were placed in a 50 ml three neck distillation flask provided with a thermometer and a vacuum distilling apparatus having a side arm. The mixture was then heated for 6 hours with stirring at a reaction temperature of 150° C. under a reduced pressure of 25 mmHg while distilling dienes which is to be produced. 7.3 g (115° to 120° C./25 mmHg) of (S)-3,7-dimethyl-5,7-octadiene-1-ol (II) was obtained in 82% yield.

후처리

  1. customprovided with a thermometer
  2. distillationa vacuum distilling apparatus
  3. temperatureThe mixture was then heated for 6 hours
  4. distillationwhile distilling dienes which
  5. customto be produced

출처 및 근거

ORD 기록
ord-29ccadfcd6a7401a9e5b97216b9481f7
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05672783

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