Methanol → Methyl acrylamidoglycolate methyl ether
Reaction equation
[C:1]([NH:5][CH:6](O)[C:7]([OH:9])=[O:8])(=[O:4])[CH:2]=[CH2:3].[CH:11]1C2NC3C(=CC=CC=3)SC=2C=CC=1.S(=O)(=O)(O)O.C(=O)([O-])[O-].[Na+].[Na+].[CH3:36][OH:37]>C(Cl)(Cl)Cl>[CH3:36][O:37][CH:6]([NH:5][C:1](=[O:4])[CH:2]=[CH2:3])[C:7]([O:9][CH3:11])=[O:8]Participants
Conditions
- Temperature
- 40 °C
Procedure
To a three-necked flask equipped with a stirrer and an extractor filled with a molecular sieve drying agent was added 300 parts acrylamidoglycolic acid, 3000 parts methanol, 0.05 parts phenothiazine, 4.5 parts 98% sulfuric acid and 200 parts chloroform. The mixture was heated to reflux and the distillate was allowed to pass through the extractor for 61/2 hours. The mixture was cooled and allowed to stand for 16 hours at which point the mixture was warmed to about 40° C., 19 g of sodium carbonate was added, and the solution was stirred for 21/2 hours. The mixture was filtered and vacuum stripped of solvent. The solid residue was extracted with chloroform. Diethyl ether was added to the extract and a polymeric mass precipitated which was discarded. The remaining extract was stripped of solvent to yield 264.2 parts of crude MAGME which was confirmed by chemical analysis.
Workup
- customTo a three-necked flask equipped with a stirrer
- additionan extractor filled with a molecular sieve drying agent
- temperatureThe mixture was heated
- temperatureto reflux
- custom2 hours
- temperatureThe mixture was cooled
- filtrationThe mixture was filtered
- extractionThe solid residue was extracted with chloroform
- additionDiethyl ether was added to the
- extractionextract
- customa polymeric mass precipitated which
- extractionThe remaining extract
Sources & evidence
- ORD record
- ord-c40a641117464e5dbf570addccf5f8fa
- Source dataset
- uspto-grants-1987_04
- Patent number
- US04656308
Reaction notes
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