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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250302Generated: October 31, 2026

Methanol → HCID 18328143, compound

https://huagongshe.com/reaction/1250302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium hydrideHCID 24758—
ReactantChlorosuccinimideHCID 31398—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 15561205HCID 15561205—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 18328143HCID 18328143—

Reaction Steps

1.0 g of 4,5-dihydro-3-methyl-1,4-benzoxazepin-5-one was dissolved in 30 ml of carbon tetrachloride, 910 mg (1.2 equivalents) of N-chlorosuccinimide was added, and the resultant mixture was agitated at 90° C. for 1 hour. This was allowed to cool, then was filtered, the filtrate was concentrated, then the resultant mixture was dissolved in 20 ml of methanol. Further, 0.86 ml (1.1 equivalents) of a methanol solution of 28% sodium methylate was added, then the resultant mixture was agitated at room temperature for 40 minutes. This was concentrated, then water was added, and extraction was performed with methylene chloride. This methylene chloride extract was washed with water and saturated saline and was dried by anhydrous magnesium sulfate, then concentrated. 368 mg of the residue was dissolved in 15 ml of dimethylformamide, then 87 mg (1.2 equivalents) of 60% sodium hydride was added under ice cooling. This was agitated for 30 minutes, then 0.64 ml (1.2 equivalents) of 1,4-dibromobutane was added, then the resultant mixture was agitated at room temperature for 3 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337397B1
Source datasetuspto-grants-2002_01
ORD IDord-37b054bf962e40ab86c64310b8caf3ad
Source noteuspto-grants-2002_01