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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723059Generated: November 2, 2026

Chlorosuccinimide → HCID 19853900, compound

https://huagongshe.com/reaction/1723059

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 numberUS04859683
Source datasetuspto-grants-1989_08
ORD IDord-ecda336a30e94d2b80bac76302b41e33
Source noteuspto-grants-1989_08