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Furan, tetrahydro-5-[(1S)-1-methoxyethyl]-3-methyl-2-(phenylthio)-, (3S,5R)-

Base Information Edit
  • Chemical Name:Furan, tetrahydro-5-[(1S)-1-methoxyethyl]-3-methyl-2-(phenylthio)-, (3S,5R)-
  • CAS No.:876152-41-9
  • Molecular Formula:C14H20O2S
  • Molecular Weight:252.378
  • Hs Code.:
  • Mol file:876152-41-9.mol
Furan, tetrahydro-5-[(1S)-1-methoxyethyl]-3-methyl-2-(phenylthio)-,
(3S,5R)-

Synonyms:

Suppliers and Price of Furan, tetrahydro-5-[(1S)-1-methoxyethyl]-3-methyl-2-(phenylthio)-, (3S,5R)-
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Chemical Property of Furan, tetrahydro-5-[(1S)-1-methoxyethyl]-3-methyl-2-(phenylthio)-, (3S,5R)- Edit
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Technology Process of Furan, tetrahydro-5-[(1S)-1-methoxyethyl]-3-methyl-2-(phenylthio)-, (3S,5R)-

There total 10 articles about Furan, tetrahydro-5-[(1S)-1-methoxyethyl]-3-methyl-2-(phenylthio)-, (3S,5R)- 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:
Multi-step reaction with 8 steps
1.1: 70 percent / DIAD; PPh3 / toluene / 16 h / 20 °C
2.1: 94 percent / KOH / ethanol / 2 h / 60 °C
3.1: 77 percent / imidazole / CH2Cl2 / 16 h / 20 °C
4.1: LDA / tetrahydrofuran / 2 h / -78 °C
4.2: tetrahydrofuran / 2 h / -78 °C
5.1: DIBAL-H / CH2Cl2 / 1 h / -78 °C
6.1: BF3*OEt2 / CH2Cl2 / 1 h / -78 °C
7.1: TBAF / tetrahydrofuran / 16 h / 20 °C
8.1: 81 percent / NaH / dimethylformamide / 2 h / 20 °C
With 1H-imidazole; potassium hydroxide; di-isopropyl azodicarboxylate; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; sodium hydride; diisobutylaluminium hydride; triphenylphosphine; lithium diisopropyl amide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; 1.1: Mitsunobu reaction;
DOI:10.1055/s-2005-918486
Guidance literature:
Multi-step reaction with 7 steps
1.1: 94 percent / KOH / ethanol / 2 h / 60 °C
2.1: 77 percent / imidazole / CH2Cl2 / 16 h / 20 °C
3.1: LDA / tetrahydrofuran / 2 h / -78 °C
3.2: tetrahydrofuran / 2 h / -78 °C
4.1: DIBAL-H / CH2Cl2 / 1 h / -78 °C
5.1: BF3*OEt2 / CH2Cl2 / 1 h / -78 °C
6.1: TBAF / tetrahydrofuran / 16 h / 20 °C
7.1: 81 percent / NaH / dimethylformamide / 2 h / 20 °C
With 1H-imidazole; potassium hydroxide; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; sodium hydride; diisobutylaluminium hydride; lithium diisopropyl amide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1055/s-2005-918486
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