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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264644Generated: October 30, 2026

N-Iodosuccinimide → tert-Butyl-{(E)-1-[2-(3-chloro-benzo[b]thiophen-2-yl)-ethyl]-3-iodo-allyloxy}-dimethylsilane

https://huagongshe.com/reaction/2264644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl-{1-[2-(3-chloro-benzo[b]thiophen-2-yl)-ethyl]-prop-2-ynyloxy}-dimethylsilaneHCID 21964439—
SolventDichloromethaneHCID 6344—
Producttert-Butyl-{(E)-1-[2-(3-chloro-benzo[b]thiophen-2-yl)-ethyl]-3-iodo-allyloxy}-dimethylsilaneHCID 2196443886.2%

Reaction Steps

A solution of alkyne 19 (5.547 g, 15.2 mmol) in dichloromethane (50 mL) was treated with Cp2ZrHCl (5.794 g, 22.5 mmol). The reaction was stirred for 45 min. and then N-iodosuccinimide (4.966 g, 22.1 mmol) was added. After 15 min., saturated sodium bicarbonate solution (200 mL) was added and the mixture was extracted with dichloromethane (2×100 mL). The combined dichloromethane solution was dried (MgSO4), filtered and evaporated. Purification by flash chromatography on silica gel (0-5% ethyl acetate/hexanes) gave 6.608 g (13.1 mmol, 86%) of the vinyl iodide (32).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855226B2
Source datasetuspto-grants-2010_12
ORD IDord-7067fb12e04f426794389a9de714a10c
Source noteuspto-grants-2010_12