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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067274Generated: November 1, 2026

Chlorosuccinimide → Ethyl 8-amino-7-chloro-2,3-dihydro-1,4-benzodioxine-5-carboxylate

https://huagongshe.com/reaction/1067274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantEthyl 8-amino-2,3-dihydro-1,4-benzodioxine-5-carboxylateHCID 15817382—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 8-amino-7-chloro-2,3-dihydro-1,4-benzodioxine-5-carboxylateHCID 1581738398.8%

Reaction Steps

37 g (0.165 mol) of ethyl 8-amino-2,3-dihydro-1,4-benzodioxine-5-carboxylate dissolved in 370 ml of dioxane are introduced into a 1 l round-bottomed flask, 23.2 g (0.174 mol) of N-chlorosuccinimide are added, at room temperature and with magnetic stirring, and the mixture is stirred overnight. It is diluted with water, extracted with ethyl acetate and, after the usual processing of the organic phase, 42 g of compound are obtained, which product is recrystallized from a mixture of diethyl ether and diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248757B1
Source datasetuspto-grants-2001_06
ORD IDord-b0bd0cfe4d194ca19f4473507599a689
Source noteuspto-grants-2001_06