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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948669Generated: October 31, 2026

Methanol → Methyl 6-fluoro-3-iodo-2-methylbenzoate

https://huagongshe.com/reaction/1948669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant6-Fluoro-3-iodo-2-methylbenzoic acidHCID 59450548—
SolventBenzeneHCID 241—
ProductMethyl 6-fluoro-3-iodo-2-methylbenzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399507B2
Source datasetuspto-grants-2013_03
ORD IDord-02f00273b72c43bfbe4c0149769ce382
Source noteuspto-grants-2013_03