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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656004Generated: November 1, 2026

HCID 86747281, compound → HCID 11412651, compound

https://huagongshe.com/reaction/1656004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86747281HCID 86747281—
SolventMethanolHCID 887—
ProductHCID 11412651HCID 11412651—

Reaction Steps

A mixture of 1.2 g, 4.2 mmol) of (Z)-O-(t-butyldimethylsilyl)-3-(t-butyldimethylsilyl)-2-propen-1-ol and 0.04 g of diisocyanate tetrabutylstannoxane [Otera, Nozaki, Tetrahedron Lett., 27, 5743 (1986)] in 140 ml of methanol is refluxed for 9 hours. Most of solvent is removed under reduced pressure and the residue is dissolved in a ether-water mixture. Etheral phase is washed with water and brine ,dried with sodium sulfate, filtered and concentrated under reduced pressure to afford 0.7 g (quantitatif crude yield) of (Z)-3-(t-butyldimethylsilyl)-2-propen-1-ol as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252587
Source datasetuspto-grants-1993_10
ORD IDord-e8f2a06fc55f4a968e27a1ef8399ed52
Source noteuspto-grants-1993_10