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2-Butynoic acid, 4-[(2R,6R)-6-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]tetrahydro-4- methylene-2H-pyran-2-yl]-, methyl ester

Base Information Edit
  • Chemical Name:2-Butynoic acid, 4-[(2R,6R)-6-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]tetrahydro-4- methylene-2H-pyran-2-yl]-, methyl ester
  • CAS No.:799852-54-3
  • Molecular Formula:C29H36O4Si
  • Molecular Weight:476.688
  • Hs Code.:
  • Mol file:799852-54-3.mol
2-Butynoic acid,
4-[(2R,6R)-6-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]tetrahydro-4-
methylene-2H-pyran-2-yl]-, methyl ester

Synonyms:

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Chemical Property of 2-Butynoic acid, 4-[(2R,6R)-6-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]tetrahydro-4- methylene-2H-pyran-2-yl]-, methyl ester Edit
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Technology Process of 2-Butynoic acid, 4-[(2R,6R)-6-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]tetrahydro-4- methylene-2H-pyran-2-yl]-, methyl ester

There total 5 articles about 2-Butynoic acid, 4-[(2R,6R)-6-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]tetrahydro-4- methylene-2H-pyran-2-yl]-, methyl ester 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:
{2-[(2R,6R)-6-(3-Bromo-prop-2-ynyl)-4-methylene-tetrahydro-pyran-2-yl]-ethoxy}-tert-butyl-diphenyl-silane; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;
methyl chloroformate; With N,N,N,N,N,N-hexamethylphosphoric triamide; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;
DOI:10.1039/b407240e
Guidance literature:
Multi-step reaction with 3 steps
1.1: PPh3 / CH2Cl2 / 0.17 h / -10 °C
1.2: 98 percent / CH2Cl2 / 0.5 h / -10 °C
2.1: 99 percent / NaHMDS / tetrahydrofuran / 1 h / -98 °C
3.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C
3.2: 86 percent / HMPA / tetrahydrofuran; hexane / 0.5 h / -78 °C
With n-butyllithium; sodium hexamethyldisilazane; triphenylphosphine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1039/b407240e
Guidance literature:
Multi-step reaction with 6 steps
1.1: 8.38 g / aq. NMO; OsO4 / tetrahydrofuran; 2-methyl-propan-2-ol / 24 h / 20 °C
2.1: PhLi / tetrahydrofuran; cyclohexane; diethyl ether / 2 h / 0 °C
2.2: 7.61 g / tetrahydrofuran; cyclohexane; diethyl ether / 3 h / -40 - -20 °C
3.1: 5.73 g / Na2CO3; Pb(OAc)4 / CH2Cl2 / 1.5 h / 0 - 20 °C
4.1: PPh3 / CH2Cl2 / 0.17 h / -10 °C
4.2: 98 percent / CH2Cl2 / 0.5 h / -10 °C
5.1: 99 percent / NaHMDS / tetrahydrofuran / 1 h / -98 °C
6.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C
6.2: 86 percent / HMPA / tetrahydrofuran; hexane / 0.5 h / -78 °C
With lead(IV) acetate; osmium(VIII) oxide; n-butyllithium; N-methyl-2-indolinone; sodium hexamethyldisilazane; sodium carbonate; phenyllithium; triphenylphosphine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; cyclohexane; tert-butyl alcohol; 2.2: Wittig methylenation;
DOI:10.1039/b407240e
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