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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729629Generated: October 30, 2026

Hydrochloric Acid → HCID 54245367, compound

https://huagongshe.com/reaction/1729629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButyl iodideHCID 10962—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57220209HCID 57220209—
SolventDimethylformamideHCID 6228—
ProductHCID 54245367HCID 54245367—

Reaction Steps

The starting material is prepared as follows: -chloro-2,3,4,5 suspension of 6.0 g of 8-chloro--tetrahydro-1-benzazepine-2,5-dione-4-carboxylic acid methyl ester in 125 ml of dimethyl formamide is added portion-wise to that of 2.1 g of a 57% mineral oil suspension of sodium hydride in 300 ml of dimethylformamide while stirring under argon. After stirring for 3 hours at room temperature 4.6 g of n-butyl iodide are added dropwise and stirring is continued over night at said temperature. The pH of the mixture is adjusted to 2 with 3N hydrochloric acid and the whole evaporated. The residue is partitioned between water and chloroform, the organic solution separated and the aqueous solution extracted with chloroform. The combined extract is washed with water, dried, evaporated and the residue taken up in diethyl ether. The mixture is treated with charcoal, filtered hot and the filtrate concentrated, to yield the 8-chloro-1-n-butyl-2,3,4,5-tetrahydro-1-benzazepine-2,5-dione-4-carboxylic acid methyl ester, melting at 89°-90°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989689
Source datasetuspto-grants-1976_11
ORD IDord-0fe7cd84d6d64d3d8217e5f992a6e6d3
Source noteuspto-grants-1976_11