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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239112Generated: October 30, 2026

Iodine → (1-benzyl-5-chloro-2,3,6,7-tetrahydro-1H-azepin-4-yl)-phenyl-methanol

https://huagongshe.com/reaction/239112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBromobenzeneHCID 7961—
ReactantMagnesiumHCID 5462224—
Reactant1-benzyl-5-chloro-2,3,6,7-tetrahydro-1H-azepine-4-carbaldehydeHCID 13072030—
SolventDiethyl EtherHCID 3283—
Product(1-benzyl-5-chloro-2,3,6,7-tetrahydro-1H-azepin-4-yl)-phenyl-methanolHCID 86686039323%

Reaction Steps

136.6 g brombenzol in 300 mL diethylether was added to 21.2 g magnesium in 100 mL diethylether. The Grignard reaction is initiated with a small amount of iodine, kept at reflux by adding the bromebenzole and stirred additional 15 min for completion. Then, 21.2 g 1-benzyl-5-chloro-2,3,6,7-tetrahydro-1H-azepine-4-carbaldehyde in 300 mL diethylether was added. The mixture was stirred 2 h at 50° C. and quenched with 200 ml 6 M HCl solution at 0° C. The reaction was filtered and the filtrate was washed with diethylether and water. The filtrate was dissolved in sodium carbonate solution and chloroform. The layers were separated and the organic layer was washed with water and evaporated to give 89.9 g of the desired product. Fp:124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642774B2
Source datasetuspto-grants-2014_02
ORD IDord-0a0ac27bdf2c408b9265ed57955699de
Source noteuspto-grants-2014_02