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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170775Generated: November 1, 2026

Propargyl bromide → HCID 59552643, compound

https://huagongshe.com/reaction/1170775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium hydrideHCID 24758—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant6-Hydroxy-1,3-benzothiazole-2-sulfonamideHCID 6852129—
SolventDimethylformamideHCID 6228—
ProductHCID 59552643HCID 5955264337.4%

Reaction Steps

To a 100 mL round bottomed flask equipped with a magnetic stir bar, rubber septum, and argon inlet containing DMF (25 mL) in an ice bath was placed 1 (17.5 g, 76.1 mmol) and the reaction was stirred at rt until the solid dissolved. To this solution was added N,N-dimethylformamide dimethyl acetal (60 g) and the mixture was heated at 40° C. for 4 h. Solvent was removed in vacuo at 42° C. and the residue was dissolved in anhydrous DMF (60 mL). To this solution at 0° C. was added portion wise NaH (4.56 g, 60% in oil, 114 mmol) and the reaction was stirred at 0° C. for 30 min. To this mixture was added propargyl bromide (18 g, 80% toluene solution, 121.7 mmol) dropwise. Ice bath was removed and the mixture was stirred at rt for 1 h. The residue was poured into a mixture of water and EtOAc (200 mL/200 mL). The mixture was filtered and solid was collected and dissolved in DCM (300 mL) and washed with saturated NaHCO3 (3×200 mL) and water (200 mL). To this solution was added 100 g of silica gel and dried in vacuo. The solid mixture was loaded on silica gel column and eluted with 10% EtOAc in DCM to afford compound 2 as a yellow solid (9.2 g, 37.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829063B2
Source datasetuspto-grants-2010_11
ORD IDord-4ec02652fc3b44ec8e53508749d26562
Source noteuspto-grants-2010_11