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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650379Generated: November 2, 2026

Chlorosuccinimide → HCID 19853900, compound

https://huagongshe.com/reaction/1650379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 14502105HCID 14502105—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 19853900HCID 19853900—

Reaction Steps

To a solution of 5 g (19.0 mmol) of methyl 6-acetylamino-2,3,4,5-tetrahydro-1-benzoxepin-9-carboxylate from Example 26 in 10 ml DMF is added 3.0 g (22.8 mmol) of N-chlorosuccinimide in a single portion at room temperature. The resulting solution is allowed to stir 24 hours at room temperature. The reaction mixture is diluted with ethyl acetate and washed with water. The organic layer is dried over MgSO4, filtered, concentrated and subjected to flash chromatography (20% EtOAc/hexanes) to yield methyl 6-acetylamino-7-chloro-2,3,4,5-tetrahydro-1-benzoxepin-9-carboxylate. This is used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04924010
Source datasetuspto-grants-1990_05
ORD IDord-5b0dde3983e14bd88069ec982c413e00
Source noteuspto-grants-1990_05