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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035143Generated: October 27, 2026

Hydrochloric Acid → 8-Bromo-7-hydroxy-1-isopropyl-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/1035143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantN-Trifluoroacetyl-8-bromo-7-hydroxy-1-isopropyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 22292823—
SolventMethanolHCID 887—
Product8-Bromo-7-hydroxy-1-isopropyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 1046908397.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of N-trifluoroacetyl-8-bromo-7-hydroxy-1-isopropyl-2,3,4,5-tetrahydro-1H-3-benzazepine (0.018 g, 0.047 mmol) in methanol (1 mL) was treated with 15% aqueous NaOH (1 mL), and stirred for 3 hours at 50° C. The product mixture was brought to pH 7-8 with 10% aqueous HCl, extracted three times with EtOAc (50 mL), dried with MgSO4, and concentrated to give 0.013 g of a white solid. 1H NMR (400 MHz, CD3OD) δ 7.10 (s, 1H), 6.60 (s, 1H), 3.30 (m, 1H), 3.2-3.0 (m, 2H), 2.78 (m, 1H), 2.7-2.5 (m, 2H), 2.3-2.1 (m, 2H), 1.05 (d, 3H), 0.73 (d, 3H). MS calculated for C13H18BrNO+H: 284, observed: 284.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546378B2
Source datasetuspto-grants-2013_10
ORD IDord-782a06b75d1e4f2d8774e88deac866ef
Source noteuspto-grants-2013_10