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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303469Generated: October 31, 2026

Chloroacetonitrile → HCID 69910038, compound

https://huagongshe.com/reaction/2303469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-hydroxy-4-(methylsulfonyl)benzoateHCID 69908919—
SolventDimethylformamideHCID 6228—
ProductHCID 69910038HCID 69910038—

Reaction Conditions

Temperature75 °C

Reaction Steps

A stirring solution of 11 (6.0 g) in DMF (200 mL) was treated with K2CO3 (6 g) and chloroacetonitrile (6 mL) and heated at 75° C. overnight. The mixture was cooled and partitioned between 1:1 EtOAc/hexanes and H2O. The organic layer was washed with 1 M NaOH, washed with brine, dried (MgSO4), filtered, and evaporated. The residue was triturated with Et2O/hexanes. The resulting solid was collected by filtration giving 6.6 g of 2-cyanomethoxy-4-methanesulfonyl-benzoic acid ethyl ester 12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433005B1
Source datasetuspto-grants-2002_08
ORD IDord-bf1baaea904c47a1bab9fabf6e29ef75
Source noteuspto-grants-2002_08