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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379822Generated: October 30, 2026

Methanesulfonic Acid → 1,3,4,5-Tetrahydro-2H-1-benzazepin-2-one

https://huagongshe.com/reaction/1379822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantN-(3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamineHCID 76876—
Product1,3,4,5-Tetrahydro-2H-1-benzazepin-2-oneHCID 24858095%

Reaction Conditions

Temperature90 °C

Reaction Steps

To 10 L of methanesulfonic acid in a 22 L 3-neck flask equipped with an overhead stirrer, a temperature probe, nitrogen inlet and reflux condenser, was added 2.6 Kg (18.61 mol) of phosphorus pentoxide. An additional 1.6 L of methanesulfonic acid was used to wash all the phosphorus pentoxide into the vessel. The mixture was heated at 90° C. for 2.5 hours then cooled to 50° C. using an ice bath and treated with 2.00 Kg (12.41 mol) of 1-tetralone oxime in several portions over 15 minutes. The mixture was heated at 63° C. for 10 minutes then slowly heated to 80° C. and kept at 80° C. for 3 hours. The reaction mixture was pumped into 70 L of ice then treated slowly with 11.25 L of 50% aqueous sodium hydroxide over 90 minutes at such a rate so as to maintain the temperature below 28° C. The mixture was filtered and 4 L of the filtrate was used to rinse the vessel. The wet cake (pink) was washed with 8 L of water then suction dried for 45 minutes and transferred to two trays and dried under vacuum at 40° C. for 2 days to give 1.9 Kg (11.79 mol,95%) of product. 1H NMR (250 MHz,CDCl3): δ 2.24 (m, 2H), 2.38 (t, 6 Hz, 2H), 2.82 (t, 6 Hz, 2H), 7.03 (d, 8 Hz, 1H), 7.13 (m, 1H), 7.24 (m, 2H), 8.63 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05672596
Source datasetuspto-grants-1997_09
ORD IDord-a9305047374c412690a68ff0ac7a10e2
Source noteuspto-grants-1997_09