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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725975Generated: October 31, 2026

Acetic Acid → HCID 11521576, compound

https://huagongshe.com/reaction/1725975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzeneHCID 241—
ReactantMethanolHCID 887—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrimethylsilyldiazomethaneHCID 167693—
CatalystAdams' catalystHCID 345198—
SolventDichloromethaneHCID 6344—
ProductHCID 11521576HCID 1152157691%

Reaction Steps

A 500 mL RB flask was charged with Example 128B (13.66 g, 47.54 mmol), benzene (190 mL), and MeOH (48 mL). To this stirred solution under N2 was added TMSCHN2 (30.9 mL, 61.81 mmol, 2.0M solution in hexanes). The reaction was stirred at room temperature for 1 hour, then quenched with 3 mL glacial AcOH. The solvent was evaporated to dryness to give a residue. The residue was dissolved in 150 mL AcOH. PtO2 (7.00 g) was added to a 500 mL reaction vessel for a Parr shaker, then purged with Ar. The solution of the residue in AcOH was then added. The vessel was fitted to the Parr shaker and charged with H2 to 60 psi (fill and vent 3×). The shaker was run for 3 hours, then filtered and evaporated to dryness to yield a solid residue. A 500 mL RB flask was charged with the residue and CH2Cl2 (154 mL). To this flask was added TFA (26 mL). The reaction was stirred for 3 hours, then transferred to a separatory funnel. The organic layer was washed with NaOH (2×250 mL) and brine (200 mL), dried over MgSO4, filtered, and evaporated to dryness to give the desired product (8.72 g, 91%). MS (ESI+Q1MS) m/e 206 (M+H)+; 1H-NMR (DMSO) δ 6.83 (d, 1H), 6.52 (d, 2H), 5.26 (s, 2H), 3.78 (s, 3H), 2.62 (m, 2H), 2.56 (m, 2H), 1.63 (quint., 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491718B2
Source datasetuspto-grants-2009_02
ORD IDord-1ef3c5218d3d428c8d380fff2c15fc47
Source noteuspto-grants-2009_02