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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891360Generated: November 2, 2026

Water → 1-(3-nitro-4-chloro-benzenesulfonyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepine

https://huagongshe.com/reaction/1891360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,3,4,5-tetrahydro-1H-1-benzazepineHCID 576503—
SolventDichloromethaneHCID 6344—
Product1-(3-nitro-4-chloro-benzenesulfonyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepineHCID 2312005890.9%

Reaction Steps

To 4-chloro-3-nitrobenzenesulfonyl chloride (1.0 g, 3.9 mmol) in dry DCM (10 mL), was added 2,3,4,5-tetrahydro-1H-benzo[b]azepine (0.57 g, 3.9 mmol). Diisopropylethylamine (1.3 mL, 7.8 mmol) was added and the mixture was stirred at ambient temperature for 16 hrs. DCM (20 mL) and 30 mL of water were added. The DCM layer was separated, washed with brine (20 mL×2), dried over MgSO4 and evaporated to give 1-(3-nitro-4-chloro-benzenesulfonyl)-2,3,4,5-tetrahydro-1H-benzo[b]azepine 4-1 as a yellow solid (1.3 g, 85% yield). MS: 367 (M+H)+; tR=2.98 min (method 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507536B2
Source datasetuspto-grants-2013_08
ORD IDord-10503aa268a94f3485bb069289a5ad53
Source noteuspto-grants-2013_08