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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459597Generated: November 4, 2026

Sodium Hydroxide → Methyl-6-methoxy-2-phenyl-5-benzothiazolcarboxylate

https://huagongshe.com/reaction/1459597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl-2-methoxy-5-benzthioamido-benzoateHCID 86753484—
CatalystHCID 178511488HCID 178511488—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl-6-methoxy-2-phenyl-5-benzothiazolcarboxylateHCID 22620051—

Reaction Conditions

Temperature55 °C

Reaction Steps

A 2 liter round bottom flask was charged with 81 grams (246 mmol) potassium ferricyanide in 300 mL of water, the solution was warmed to 55° C. A solution of 14.78 grams (49 mmol) methyl-2-methoxy-5-benzthioamido-benzoate in 200 mL of methanol and 100 mL aqueous sodium hydroxide solution [13.7 gm (343 mmol) NaOH/100 mL] was then added. A yellow precipitate was soon deposited. The mixture was stirred at 60° C. for 1.5 hours. The reaction mixture was partitioned between 1 liter ethyl acetate and 300 mL 3.4N HCl (aqueous). The organic phase was washed with water and brine solution and then dried over sodium sulfate. After filtration, the filtrate was evaporated and the residue, as a mixture of carboxylates, was used directly in the next step. (affords 12.9 grams crude)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854262
Source datasetuspto-grants-1998_12
ORD IDord-96a8ec548ca2422b9d9b1f2b0da0acaa
Source noteuspto-grants-1998_12