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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732926Generated: November 1, 2026

Methyl iodide → HCID 12848219, compound

https://huagongshe.com/reaction/1732926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 12581860HCID 12581860—
ReactantHCID 12703381HCID 12703381—
SolventEthanolHCID 702—
ProductHCID 12848219HCID 12848219—
ProductHCID 178421795HCID 178421795—

Reaction Steps

The starting material, thieno[3,4-b][1,5]benzoxazepin-10(9H)-one (I) or 7-methyl-thieno[3,4-b][1,5]benzoxazepin-10(9H)-one (II) in ethanol is treated with sodium methoxide and methyl iodide and extracted with methylene chloride to yield 9-methyl-thieno[3,4-b][1,5]benzoxazepin-10(9H)-one (III) and 7,9-dimethyl-thieno[3,4][1,5]benzoxazepin-10(9H)-one (IV) respectively. The above compounds III and IV are refluxed with 5 N sodium hydroxide for 16 hours, diluted with water, adjusted to pH 4-5 with hydrochloric acid and extracted with methylene chloride. The base compounds thus obtained are dissolved in ether and treated with alcoholic hydrochloric acid to give the corresponding 4-(o-methylaminophenoxy)-3-thiophenecarboxylic acid hydrochloride (V) and 4-(2-methylamino-p-tolyloxy)-3-thiophenecarboxylic acid hydrochloride (VI) compounds.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04239898
Source datasetuspto-grants-1980_12
ORD IDord-671e9dca96ea48ce834f8a30b81c9120
Source noteuspto-grants-1980_12