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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637178Generated: October 30, 2026

Water → 2-((3-Chlorophenyl)carbonyl)amino-5-nitroindane

https://huagongshe.com/reaction/1637178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
Reactant5-Nitro-indan-2-ylamine hydrochlorideHCID 22319324—
SolventDichloromethaneHCID 6344—
Product2-((3-Chlorophenyl)carbonyl)amino-5-nitroindaneHCID 23298399—

Reaction Steps

To 2-amino-5-nitroindane hydrochloride (1.5 g, 7.0 mmol) in methylene chloride (50 ml) at 0° C. was added triethylamine (2.1 ml, 15.0 mmol) follwed by 3-chlorobenzoyl chloride (1.0 ml, 7.5 mmol). The mixture was dumped immediately into water and the layers separated. The aqueous layer was extracted with methylene chloride (2×20 ml) and the combined extracts washed with water, dried over MgSO4, filtered, and concentrated to an oil which was homogeneous by TLC and used immediately in the next step: M.S. (M+H)+ =317.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040314
Source datasetuspto-grants-2000_03
ORD IDord-888b99650a6845a6aafaa25f2b3c65e1
Source noteuspto-grants-2000_03