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1H-Isoindol-1-one, 2,3-dihydro-2-[(1R)-2-hydroxy-1-[4-(phenylmethoxy)phenyl]ethyl]-3-prop yl-, (3R)-

Base Information
  • Chemical Name:1H-Isoindol-1-one, 2,3-dihydro-2-[(1R)-2-hydroxy-1-[4-(phenylmethoxy)phenyl]ethyl]-3-prop yl-, (3R)-
  • CAS No.:677009-88-0
  • Molecular Formula:C26H27NO3
  • Molecular Weight:401.505
  • Hs Code.:
1H-Isoindol-1-one,
2,3-dihydro-2-[(1R)-2-hydroxy-1-[4-(phenylmethoxy)phenyl]ethyl]-3-prop
yl-, (3R)-

Synonyms:

Suppliers and Price of 1H-Isoindol-1-one, 2,3-dihydro-2-[(1R)-2-hydroxy-1-[4-(phenylmethoxy)phenyl]ethyl]-3-prop yl-, (3R)-
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Chemical Property of 1H-Isoindol-1-one, 2,3-dihydro-2-[(1R)-2-hydroxy-1-[4-(phenylmethoxy)phenyl]ethyl]-3-prop yl-, (3R)-
Chemical Property:
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Technology Process of 1H-Isoindol-1-one, 2,3-dihydro-2-[(1R)-2-hydroxy-1-[4-(phenylmethoxy)phenyl]ethyl]-3-prop yl-, (3R)-

There total 3 articles about 1H-Isoindol-1-one, 2,3-dihydro-2-[(1R)-2-hydroxy-1-[4-(phenylmethoxy)phenyl]ethyl]-3-prop yl-, (3R)- 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 4 steps
1: LiAlH4 / tetrahydrofuran / Heating
2: 79 percent / 15 h / 170 - 180 °C
3: 93 percent / diethyl ether; CH2Cl2 / 4 h / -15 - -10 °C
4: Et3SiH; BF3*OEt2 / CH2Cl2 / 6 h / -78 °C
With triethylsilane; lithium aluminium tetrahydride; boron trifluoride diethyl etherate; In tetrahydrofuran; diethyl ether; dichloromethane; 3: Grignard reaction;
DOI:10.1016/j.tet.2003.11.092
Guidance literature:
Multi-step reaction with 3 steps
1: 79 percent / 15 h / 170 - 180 °C
2: 93 percent / diethyl ether; CH2Cl2 / 4 h / -15 - -10 °C
3: Et3SiH; BF3*OEt2 / CH2Cl2 / 6 h / -78 °C
With triethylsilane; boron trifluoride diethyl etherate; In diethyl ether; dichloromethane; 2: Grignard reaction;
DOI:10.1016/j.tet.2003.11.092
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