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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035120Generated: October 30, 2026

Sodium Hydroxide → 7-Allyloxy-8-bromo-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/1035120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22292776HCID 22292776—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-Allyloxy-8-bromo-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 1033471899%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of N-trifluoroacetyl-7-allyloxy-8-bromo-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (1.18 g, 3.00 mmol) in methanol (35 mL) was treated with 15% aqueous NaOH (35 mL), and stirred overnight at 20° C. The product mixture was diluted with water (200 mL), extracted twice with EtOAc (200 mL), the combined organic phases were washed with brine (100 mL), dried with Na2SO4 and concentrated to give 0.880 g of a clear oil. 1H NMR (400 MHz, CDCl3) δ 7.29 (s, 1H), 6.63 (s, 1H), 6.04 (m, 1H), 5.47 (d, J=17 Hz, 1H), 5.29 (d, J=11 Hz, 1H), 4.58 (s, 2H), 3.01 (m, 3H), 2.89 (m, 3H), 2.75 (m, 1H), 1.31 (d, J=7 Hz, 3H). MS calculated for C14H18BrNO+H: 296, observed: 296.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546378B2
Source datasetuspto-grants-2013_10
ORD IDord-fda12f2de4d84a6692fd0dafc589842c
Source noteuspto-grants-2013_10