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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044372Generated: October 30, 2026

tert-Butanol → HCID 178426227, compound

https://huagongshe.com/reaction/1044372

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant18-Crown-6HCID 28557—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantBenzene, 2-fluoro-1-iodo-4-methyl-HCID 2774524—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 178517864HCID 178517864—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 178426227HCID 178426227—

Reaction Steps

A mixture of (5S)-2-(trans-4-hydroxycyclohexyl)-2,7-diazaspiro[4.5]decan-1-one (20 mg, 0.00007 mol) which was prepared using procedures analogous to those described in the synthesis of example 472-a and followed by standard hydrogenation to remove the carbobenzyloxy (Cbz) protecting and, 4-methyl-2-fluoro-1-iodobenzene (21 mg, 0.00009 mol), sodium tert-butoxide (9.98 mg, 0.000104 mol), 1,4,7,10,13,16-hexaoxacyclooctadecane (27.4 mg, 0.000104 mol), 2-(di-tert-butylphosphino)biphenyl (0.8 mg, 0.000003 mol), tris(dibenzylideneacetone)dipalladium(0) (1 mg, 0.000001 mol), in tert-butyl alcohol (1.0 mL, 0.010 mol) was stirred at rt for 18. The crude product was purified by prep-HPLC to afford the desired product. LC-MS: 361.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563570B2
Source datasetuspto-grants-2013_10
ORD IDord-e18d147941634d9a909532e523b49ff0
Source noteuspto-grants-2013_10