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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854973Generated: October 29, 2026

Propargyl bromide → HCID 58934812, compound

https://huagongshe.com/reaction/854973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium HydroxideHCID 14798—
Reactant7-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylic acidHCID 69519064—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHCID 178418397HCID 178418397—
ProductHCID 58934812HCID 5893481240%

Reaction Steps

To a suspension of (9-BBN)2 (1.96 g, 8.7 mmol) in 10 mL THF was added propargyl bromide (0.53 g, 4.4 mmol). After heating for 2 h and cooling to room temperature, NaOH (0.52 g, 13 mmol) in 4.3 mL of H2O was added and the reaction was stirred for 1 h. In a separate flask under argon was added the title product of Example 146 Step 1 in 5 mL of THF and Pd(PPh3)4. The reaction from the original flask was transferred to the second flask via cannula. After refluxing for 18 h and cooling to room temperature, 25 mL of H2O was added. The organic solvent was removed from the reaction under vacuum. The aqueous layer was extracted three times with 70 mL EtOAc. The combined organic extractions were washed one time with 50 mL of 1 N HCl and one time with 50 mL of saturated brine. Following drying over MgSO4 and concentrating under vacuum, the product was purified by flash column chromatography and reverse phase chromatography on YMC ODS-AQ in MeOH/H2O to yield desired product (0.40 g, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-e27ffc9b4e7043099cd1134ce02a3beb
Source noteuspto-grants-2007_08