HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthoformate → 1-Dimethoxymethyl-5-fluoro-2-methoxy-4-nitro-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 5-Fluoro-2-methoxy-4-nitrobenzaldehyde | HCID 86222845 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Dimethoxymethyl-5-fluoro-2-methoxy-4-nitro-benzene | HCID 67426673 | — |
Reaction Steps
A mixture of 0.210 g (1.06 mmole) of 5-fluoro-2-methoxy-4-nitro-benzaldehyde (IV.46c), 1 mL of trimethylorthoformate, 0.025 g of p-toluenesulfonic acid monohydrate and 5 mL of methanol was heated at reflux for one hour. The mixture was cooled, neutralized by addition of saturated sodium bicarbonate solution and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and saturated sodium bicarbonate solution. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 0.243 g of 1-dimethoxymethyl-5-fluoro-2-methoxy-4-nitro-benzene (IV.46d) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044213B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-7c1f0805e1364af38007b03c0827af1c |
| Source note | uspto-grants-2011_10 |