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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645384Generated: October 30, 2026

Chlorosuccinimide → HCID 24773647, compound

https://huagongshe.com/reaction/645384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 86613107HCID 86613107—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 24773647HCID 2477364711.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of (S)-N-Trifluoroacetyl-8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (0.62 g, 2.1 mmol) in dichloromethane (10 mL) was treated with N-chlorosuccinimide (0.284 g, 2.1 mmol) and trifluoromethanesulfonic acid (0.639 g, 4.2 mmol). The reaction was stirred for 16 h at 20° C., diluted with water (20 mL) and extracted with dichloromethane (25 mL). The organics were dried with MgSO4, filtered and concentrated. HPLC purification was done to provide 0.078 g of a white solid. 1H NMR (400 MHz, CDCl3, mixture of rotamers) δ 7.32-7.25 (m, 1H), 6.97-6.93 (m, 1H), 4.27-4.24 (m, 0.6H), 4.19-4.13 (m, 1H), 4.08-4.01 (m, 1H), 3.91-3.86 (0.8H, m), 3.74-3.69 (m, 0.8H:), 3.45-3.37 (m, 1H), 3.31-3.21 (m, 1H), 2.96-2.80 (m, 1H), 1.28-1.22 (m, 3H). MS calculated for C13H12Cl2F3NO+H: 326, observed: 326.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704993B2
Source datasetuspto-grants-2010_04
ORD IDord-3dfebf32e06443f5843e79e43dff5a51
Source noteuspto-grants-2010_04