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1,3-Dioxolane, 2,2-dimethyl-4-(1-propynyl)-, (4R)- (9CI)

Base Information Edit
  • Chemical Name:1,3-Dioxolane, 2,2-dimethyl-4-(1-propynyl)-, (4R)- (9CI)
  • CAS No.:710324-25-7
  • Molecular Formula:C8H12 O2
  • Molecular Weight:140.182
  • Hs Code.:
  • Mol file:710324-25-7.mol
1,3-Dioxolane, 2,2-dimethyl-4-(1-propynyl)-, (4R)- (9CI)

Synonyms:1,3-Dioxolane,2,2-dimethyl-4-(1-propynyl)-, (4R)- (9CI)

Suppliers and Price of 1,3-Dioxolane, 2,2-dimethyl-4-(1-propynyl)-, (4R)- (9CI)
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 1 raw suppliers
Chemical Property of 1,3-Dioxolane, 2,2-dimethyl-4-(1-propynyl)-, (4R)- (9CI) Edit
Chemical Property:
  • PSA:18.46000 
  • LogP:1.16120 
Purity/Quality:

99%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
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Technology Process of 1,3-Dioxolane, 2,2-dimethyl-4-(1-propynyl)-, (4R)- (9CI)

There total 2 articles about 1,3-Dioxolane, 2,2-dimethyl-4-(1-propynyl)-, (4R)- (9CI) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
(R)-(+)-4-(2,2-Dibromoethenyl)-2,2-dimethyl-1,3-dioxolane; With n-butyllithium; In tetrahydrofuran; hexane; at -78 - -20 ℃; for 3h;
methyl iodide; In tetrahydrofuran; hexane; at -20 - 20 ℃; Further stages.;
DOI:10.1039/b209573d
Guidance literature:
Multi-step reaction with 2 steps
1.1: Zn; triphenylphosphine / CH2Cl2 / 48 h / 0 °C
1.2: 61 percent / CH2Cl2 / 2 h
2.1: n-BuLi / tetrahydrofuran; hexane / 3 h / -78 - -20 °C
2.2: tetrahydrofuran; hexane / -20 - 20 °C
With n-butyllithium; triphenylphosphine; zinc; In tetrahydrofuran; hexane; dichloromethane; 1.1: Corey-Fuchs reaction;
DOI:10.1039/b209573d
Guidance literature:
Multi-step reaction with 4 steps
1: 81 percent / aq. AcOH / 4 h / 20 °C
2: 814 mg / sulfuric acid / 1 h / 20 °C
3: 10 percent / potassium permanganate; MgSO4; NaHCO3 / acetone; H2O / 0.33 h / 20 °C
4: H2O; aq. phosphate buffer; NaCl / 36 h / pH 6.5
With potassium permanganate; phosphate buffer; sulfuric acid; water; sodium hydrogencarbonate; magnesium sulfate; acetic acid; sodium chloride; In water; acetone;
DOI:10.1002/anie.200353150
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