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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863376Generated: October 25, 2026

2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide → HCID 178509799, compound

https://huagongshe.com/reaction/863376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromideHCID 2724168—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178509801HCID 178509801—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178509799HCID 17850979989.3%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A mixture of (2-(1,3-dioxan-2-yl)ethyl)triphenylphosphonium bromide (25.0 g, 54.7 millimols) with THF (150 ml) was cooled down to -20° C., followed by adding t-BuOK (6.1 g, 54.7 millimols) to the mixture, stirring for 30 minutes, dropwise adding to the mixture, a THF (80 ml) solution of trans-4-(trans-4-(4-cyanophenyl)cyclohexyl)cyclohexanecarbaldehyde (14.4 g, 49.8 millimols) so as to keep the temperature at -20° C. or lower, stirring the mixture at the same temperature for 2 hours, and treating the reaction product in the same manner as in Example 2, except that the quantity of ethyl acetate used for extraction was made 400 ml, to obtain raw 4-(trans-4-(trans-4-(3-(1,3-dioxan-2-yl)propenyl)cyclohexyl)cyclohexyl)benzonitrile (17.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05720899
Source datasetuspto-grants-1998_02
ORD IDord-a1349c1cfa6d421c9be6f9bfbae78a1e
Source noteuspto-grants-1998_02