HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → N-Methyl-5-nitro-isophthalamic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Ethyl 3-(chlorocarbonyl)-5-nitrobenzoate | HCID 3023043 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Methyl-5-nitro-isophthalamic acid ethyl ester | HCID 47099901 | — |
Reaction Steps
To a 2M solution of methylamine in THF (256 ml) at −20° C. was added a pre-cooled solution of 3-chlorocarbonyl-5-nitro-benzoic acid ethyl ester (60 g) in THF (500 ml) dropwise. This was stirred for 20 min and then filtered. The filtrate was concentrated in vacuum and the solid recrystallised from diethyl ether to give the title compound (22.5 g) as a solid. An oxalyl chloride solution in DCM (63 ml, 2M), was added with DMF (5 ml). The reaction was stirred for 2 h and then concentrated in vacuum. The residue was triturated with toluene and again concentrated in vacuum leaving the title compound (60 g). Rt=1.53 min (method D).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE045323E1 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-e13cc62fd39e4d038af6210ca3511aa9 |
| Source note | uspto-grants-2015_01 |