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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133167Generated: October 29, 2026

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

https://huagongshe.com/reaction/133167

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 A3 (6.5 g) was dissolved in THF (100 mL) and added to a solution of DIBAL (70 mL, 1M in hexanes) (available from Aldrich) in THF (160 mL) at −35° C. for 35 m. 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 m at rt. 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 A4) 3.6 g (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390829B2
Source datasetuspto-grants-2008_06
ORD IDord-42d804f4b7024545b7f03089cd754f3b
Source noteuspto-grants-2008_06