Technology Process of D-3-iodo-4,5-diisopropyloxyphenyl glycine methyl ester
There total 8 articles about D-3-iodo-4,5-diisopropyloxyphenyl glycine 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:
-
Multi-step reaction with 2 steps
1: aq. NaHCO3; KBr; NaOCl / TEMPO / acetone / 1.5 h / 0 °C
2: SOCl2 / 12 h / 20 °C
With
sodium hypochlorite; thionyl chloride; sodium hydrogencarbonate; potassium bromide;
2,2,6,6-tetramethyl-piperidine-N-oxyl;
In
acetone;
DOI:10.1021/ol070889p
- Guidance literature:
-
Multi-step reaction with 3 steps
1: n-Bu4NF / tetrahydrofuran / 2 h / 0 °C
2: aq. NaHCO3; KBr; NaOCl / TEMPO / acetone / 1.5 h / 0 °C
3: SOCl2 / 12 h / 20 °C
With
sodium hypochlorite; thionyl chloride; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; potassium bromide;
2,2,6,6-tetramethyl-piperidine-N-oxyl;
In
tetrahydrofuran; acetone;
DOI:10.1021/ol070889p
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: AD-mix-α / 2-methyl-propan-2-ol; H2O / 6 h / 25 °C
1.2: imidazole / dimethylformamide / 5 h / 0 °C
1.3: triphenylphosphine; diisopropyl azodicarboxylate; diphenylphosphoryl azide / tetrahydrofuran / 2 h / 0 °C
2.1: triphenylphosphine / tetrahydrofuran; H2O / 3 h / 60 °C
3.1: Et3N / CH2Cl2 / 20 °C
4.1: n-Bu4NF / tetrahydrofuran / 2 h / 0 °C
5.1: aq. NaHCO3; KBr; NaOCl / TEMPO / acetone / 1.5 h / 0 °C
6.1: SOCl2 / 12 h / 20 °C
With
sodium hypochlorite; AD-mix-α; thionyl chloride; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; triethylamine; triphenylphosphine; potassium bromide;
2,2,6,6-tetramethyl-piperidine-N-oxyl;
In
tetrahydrofuran; dichloromethane; water; acetone; tert-butyl alcohol;
1.1: Sharpless asymmetric dihydroxylation / 1.3: Mitsunobu reaction;
DOI:10.1021/ol070889p