HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 6-fluoro-3-iodo-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 6-Fluoro-3-iodo-2-methylbenzoic acid | HCID 59450548 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Methyl 6-fluoro-3-iodo-2-methylbenzoate | HCID 59450535 | — |
Reaction Steps
Trimethylsilyldiazomethane solution (2 M in Hexane) (18 mL, 35 mmol) was added dropwise to a stirred solution of the product of Step A (7.3 g, 33.2 mmol) in benzene containing 20% of methanol (total: 100 mL) at room temperature until solution retained a yellow color. The mixture was concentrated to remove the organic solvent. The remaining oil was poured over a silica gel plug in a 60-mL filter frit funnel and eluting with 200 mL of hexane containing 10% ethyl acetate. The filtrate was then concentrated to dryness to give the title compound as a bright yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399507B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-02f00273b72c43bfbe4c0149769ce382 |
| Source note | uspto-grants-2013_03 |