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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910790Generated: October 28, 2026

Triethylamine → [5-(2-Benzyloxy-ethyl)-cyclohex-1-enylmethoxy]-tert-butyl-dimethyl-silane

https://huagongshe.com/reaction/910790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant{5-[2-(Benzyloxy)ethyl]cyclohex-1-en-1-yl}methanolHCID 21879600—
SolventDimethylformamideHCID 6228—
Product[5-(2-Benzyloxy-ethyl)-cyclohex-1-enylmethoxy]-tert-butyl-dimethyl-silaneHCID 2187959863%

Reaction Steps

Intermediate R3 was dissolved in THF (100 mL) and added to a solution of DIBAL (70 mL, 1M in hexanes) in THF (160 mL) at −35° C. for 35 minutes. The mixture was quenched with Rochelle's salt solution, and extracted with ether. The dried residue was purified by chromatography on SiO2 with 30% EtOAc:Hx to yield [5-(2-benzyloxy-ethyl)-cyclohex-1-enyl]-methanol 4.6 g (80%). A solution of the alcohol (4.0 g, 18.7 mmol) in DMF (60 mL) was treated with triethylamine (3 mL) followed by TBSCl (3.0 g, 22.4 mol) for 20 minutes at room temperature. The residue was isolated from an aqueous work-up and purified by chromatography to give [5-(2-benzyloxy-ethyl)-cyclohex-1-enylmethoxy]-tert-butyl-dimethyl-silane (Intermediate R4) 3.6 g (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022226B2
Source datasetuspto-grants-2011_09
ORD IDord-4091888ca1f74080969602d017fad085
Source noteuspto-grants-2011_09