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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543237Generated: October 30, 2026

Propargyl alcohol → HCID 20205910, compound

https://huagongshe.com/reaction/543237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-benzamido-3-(1H-indol-3-yl)propanoic acidHCID 294891—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 20205910HCID 20205910—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(benzoylamino)-3-(indol-3-yl)propanoic acid (1.9 g) was dissolved in 75 ml of dry methylene chloride (from phosphorous pentoxide). The solution was cooled to 0° C. in an ice bath and 0.72 ml of propargyl alcohol was added along with 1.39 g of DCC followed by 0.07 g DMAP. The reaction mixture was warmed to room temperature and maintained there for 16 hours. The solution was filtered into a separatory funnel, washed with 5% acetic acid (2×), water (1×) and 5% solution bicarbonate (1×). The separated methylene chloride layer was then dried over magnesium sulfate and evaporated to dryness. The residue was redissolved in ethyl acetate, filtered and the filtrate evaporated to dryness. The orangish residue was dried in vacuo to give propargyl 2-(benzoylamino)-3-(indol-3-yl)propionate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04661510
Source datasetuspto-grants-1987_04
ORD IDord-1d38b6c30064478e9f634029882ea6d5
Source noteuspto-grants-1987_04