HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 3-[(2-Methoxyethyl)(methyl)amino]-2-methyl-4-(methylsulfonyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-[(2-Methoxyethyl)amino]-2-methyl-4-(methylsulfonyl)benzoic acid | HCID 69116726 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[(2-Methoxyethyl)(methyl)amino]-2-methyl-4-(methylsulfonyl)benzoic acid | HCID 69117785 | — |
Reaction Steps
Under nitrogen, 1.0 g (3 mmol) of 3-[(2-methoxyethyl)amino]-2-methyl-4-(methylsulfonyl)benzoic acid was dissolved in 150 ml of THF, and 10 g of paraformaldehyde and then, a little at a time, 0.7 g (20 mmol) of NaBH4 were added. 15 ml of trifluoroacetic acid were then slowly added dropwise. The mixture was stirred at RT for another 3 days. For work-up, 10% strength H2SO4 was added, and the mixture was extracted repeatedly with EA and then dried over MgSO4 and concentrated. This gave a brownish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07396939B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-2809dc99cb6842e1999bc37d719c7038 |
| Source note | uspto-grants-2008_07 |