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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063456Generated: November 1, 2026

Water → HCID 69338646, compound

https://huagongshe.com/reaction/1063456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropargyl alcoholHCID 7859—
ReactantTriethylamineHCID 8471—
ReactantHCID 69338013HCID 69338013—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductHCID 69338646HCID 6933864654%

Reaction Conditions

Temperature80 °C

Reaction Steps

(2R)-Acetylamino-2-methyl-4-(5-bromothiophen-2-yl)butyl acetate (1.38 g, 3.95 mmol) obtained in Example 47 (c) was dissolved in dimethylformamide (20 ml), and then propargylalcohol (0.69 ml, 11.9 mmol), triethylamine (5.60 ml, 40.1 mmol), copper(I) iodide (76 mg, 0.40 mmol), and dichlorobis(triphenylphosphine)palladium (276 mg, 0.39 mmol) were added thereto followed by stirring for 1 hour at 80° C. under a nitrogen atmosphere. The reaction solution was poured into water, extracted with ethyl acetate, and after the ethyl acetate layer was dried over anhydrous sodium sulfate, the solvent was evaporated in vacuo. The residue was purified by chromatography on a silica gel column (elution solvent; hexane:ethyl acetate=3:1-1:3) to afford the title compound (685 mg, 54% yield) as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964976B2
Source datasetuspto-grants-2005_11
ORD IDord-9afe3f62c1e945699fdb30c761edc47c
Source noteuspto-grants-2005_11