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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33203Generated: October 29, 2026

Methyl iodide → 3-Acetyl-7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/33203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
Reactant3-acetyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7-sulfonyl chlorideHCID 11346737—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Acetyl-7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 1126563473.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a stirred solution of sodium sulphite (1.60 g, 12.6 mmol) and sodium hydrogen carbonate (1.14 g, 13.56 mmol) in water (25 ml) was added 3-acetyl-7-chlorosulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine (2.6 g, 9.04 mmol) in tetrahydrofuran (10 ml). The reaction mixture was then heated at 75° C. for 2 h, cooled to 30° C. and methyl iodide (2.8 ml, 45.20 mmol) added. After stirring at 50° C. for 24 h, the reaction mixture was cooled to room temperature and partitioned between water (50 ml) and ethyl acetate (100 ml). The aqueous layer was then separated and further extracted with ethyl acetate (2×80 ml). The combined organics were then dried (Na2SO4) and the solvent removed in vacuo to give the title compound (1.77 g, 73%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429579B2
Source datasetuspto-grants-2008_09
ORD IDord-38a99d1ea04842b5afd660197151a66f
Source noteuspto-grants-2008_09