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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035342Generated: October 29, 2026

Sodium Hydroxide → 8-Bromo-7-ethoxy-1-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

https://huagongshe.com/reaction/1035342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-Trifluoroacetyl-8-bromo-7-ethoxy-1-methyl-2,3, 4,5-tetrahydro-1H-3-benzazepineHCID 22292768—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product8-Bromo-7-ethoxy-1-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 1040160294.7%

Reaction Steps

A solution of N-trifluoroacetyl-8-bromo-7-ethoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (0.010 g, 0.026 mmol) in methanol (1 mL) was treated with 15% aqueous NaOH (1 mL), and stirred overnight at 20 C. The product mixture was diluted with water (3 mL), extracted twice with EtOAc (5 mL), the combined organic phases were washed with brine (3 mL), dried with Na2SO4 and concentrated to give 0.007 g of a clear oil. 1H NMR (400 MHz, CDCl3) d 7.29 (s, 1 H), 6.63 (s, 1 H), 4.07 (q, J=6 Hz, 2 H), 3.03 (m, 3 H), 2.91 (m, 3 H), 2.73 (m, 1 H), 2.26 (bs, 1 H), 1.46 (t, J=6 Hz, 3 H), 1.32 (d, J=7 Hz, 3 H). MS calculated for C15H17BrF3NO2+H: 380, observed: 380.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546379B2
Source datasetuspto-grants-2013_10
ORD IDord-25ebc34c35ef4a31ace27f7d53d351c9
Source noteuspto-grants-2013_10