Technology Process of Benzeneacetic acid, 4-methoxy-a-(1-methylethyl)-, (R)-
There total 4 articles about Benzeneacetic acid, 4-methoxy-a-(1-methylethyl)-, (R)- which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
(Sa,S)-[(C8H12)Ir(P(3,5-(tert-butyl)2C6H3)2C8H7CC8H7C3NOH3(benzyl))][tetrakis[3,5-bis(trifluoromethyl)phenyl]borate]; hydrogen; triethylamine;
In
methanol;
at 60 ℃;
for 20h;
under 4560.31 Torr;
enantioselective reaction;
Autoclave;
Inert atmosphere;
DOI:10.1021/ol401593a
- Guidance literature:
-
With
silver tetrafluoroborate; (S)-cyclohexyl-BINAP; hydrogen; triethylamine; rhodium(I) chloride;
In
methanol;
at 25 ℃;
for 24h;
under 38000 Torr;
Yield given. Yields of byproduct given. Title compound not separated from byproducts;
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: isopropylmagnesium chloride / tetrahydrofuran / 1.5 h / 25 - 40 °C / Inert atmosphere; Schlenk technique
1.2: Cooling with ice
2.1: triethylamine; hydrogen; (Sa,S)-[(C8H12)Ir(P(3,5-(tert-butyl)2C6H3)2C8H7CC8H7C3NOH3(benzyl))][tetrakis[3,5-bis(trifluoromethyl)phenyl]borate] / methanol / 20 h / 60 °C / 4560.31 Torr / Autoclave; Inert atmosphere
With
(Sa,S)-[(C8H12)Ir(P(3,5-(tert-butyl)2C6H3)2C8H7CC8H7C3NOH3(benzyl))][tetrakis[3,5-bis(trifluoromethyl)phenyl]borate]; hydrogen; isopropylmagnesium chloride; triethylamine;
In
tetrahydrofuran; methanol;
DOI:10.1021/ol401593a