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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689668Generated: November 1, 2026

Chlorosuccinimide → HCID 22292769, compound

https://huagongshe.com/reaction/1689668

Reaction equation

Participants

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

Reaction Conditions

Temperature70 °C

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) δ 7.17 (s, 1H), 6.68 (m, 1 H), 3.88 (s, 3H), 3.78 (m, 1H), 3.6-3.3 (m, 2H), 3.2-2.9 (m, 4H), 1.34 (m, 3H). MS calculated for C14H15ClF3NO2+H: 322, observed: 322.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153621B2
Source datasetuspto-grants-2012_04
ORD IDord-1f7ddf890f7a4701aebc909ac1adf8b9
Source noteuspto-grants-2012_04