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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749230Generated: November 1, 2026

Triethylamine → tert-Butyl-{1-[2-(3-chloro-benzo[b]thiophen-2-yl)-ethyl]-prop-2-ynyloxy}-dimethylsilane

https://huagongshe.com/reaction/1749230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(3-Chloro-benzo[b]thiophen-2-yl)-pent-1-yn-3-olHCID 21964427—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Producttert-Butyl-{1-[2-(3-chloro-benzo[b]thiophen-2-yl)-ethyl]-prop-2-ynyloxy}-dimethylsilaneHCID 2196443973%

Reaction Steps

A solution of alcohol 18 (2.20 g, 8.78 mmol) in dichloromethane (15 mL) was treated with DMAP (215 mg, 1.8 mmol), TBSCl (1.59 g, 10.5 mmol), and triethylamine (1.8 mL, 13.2 mmol). The reaction was stirred for 24 h and then saturated sodium bicarbonate solution (50 mL) was added. The mixture was extracted with dichloromethane (2×50 mL) and the combined dichloromethane solution dried (Na2SO4), filtered and evaporated. Purification by flash chromatography (4% ethyl acetate/hexane) gave 3.06 g (6.4 mmol, 73%) of the protected alcohol (19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156810B2
Source datasetuspto-grants-2015_10
ORD IDord-5a7a843f217f41f4b1223f844a18df9e
Source noteuspto-grants-2015_10