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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221240Generated: October 30, 2026

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

https://huagongshe.com/reaction/221240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-trifluoroacetyl-8-iodo-7-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 22292785—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product7-iodo-8-methoxy-5-methyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 1006438692.4%

Reaction Steps

A solution of N-trifluoroacetyl-8-iodo7-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (0.600 g, 1.45 mmol) in methanol (20 mL) was treated with 15% aqueous NaOH (20 mL), and stirred for 3 hours at 50 C. The product mixture was diluted with water (100 mL), extracted twice with EtOAc (100 mL), the combined organic phases were washed with brine (100 mL), dried with Na2SO4 and concentrated to give 0.425 g of a yellow solid. 1H NMR (400 MHz, CDCl3) d 7.52 (s, 1 H), 6.57 (s, 1H), 3.86 (s, 3 H), 3.12-3.06 (m, 4 H), 2.95 (m, 2 H), 2.75 (m, 1 H), 2.43 (bs, 1 H), 1.33 (d, J=8 Hz, 3 H). MS calculated for C12H16INO+H: 318, observed: 318.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207158B2
Source datasetuspto-grants-2012_06
ORD IDord-2ea3760e4bcf418cbcb2cbd472d12d41
Source noteuspto-grants-2012_06