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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967236Generated: November 1, 2026

Chlorosuccinimide → HCID 22292769, compound

https://huagongshe.com/reaction/967236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 22292800HCID 22292800—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 22292769HCID 2229276946.4%

Reaction Steps

A solution of N-trifluoroacetyl-7-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (0.900 g, 2.67 mmol) in acetonitrile (30 mL) was treated with N-chlorosuccinimide (0.357 g, 2.67 mmol) and stirred overnight at 70 C. The product mixture was diluted with water (100 mL), extracted twice with EtOAc (100 mL), the combined organic phases washed with brine (100 mL), dried with Na2SO4 and concentrated. Flash chromatography (20% EtOAc in hexane, silica) resulted in 0.399 g of a clear oil. 1H NMR (400 MHz, CDCl3, mixture of rotamers) d 7.17 (s, 1 H), 6.68 (m, 1 H), 3.88 (s, 3 H), 3.78 (m, 1 H), 3.6−3.3 (m, 2 H), 3.2−2.9 (m, 4 H), 1.34 (m, 3 H). MS calculated for C14H15ClF3NO2+H: 322, observed: 322.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953787B2
Source datasetuspto-grants-2005_10
ORD IDord-4b11cc6467b340eeb9d7fd3e5454afbf
Source noteuspto-grants-2005_10