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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261803Generated: November 1, 2026

Pivaloyl chloride → HCID 23335544, compound

https://huagongshe.com/reaction/261803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
Reactant{4-[(Oxiran-2-yl)methoxy]-1H-indol-2-yl}methanolHCID 14044141—
SolventPyridineHCID 1049—
ProductHCID 23335544HCID 23335544—

Reaction Steps

11.5 g. 4-(2,3-epoxypropoxy)-2-hydroxymethyl-indole (see U.S. Pat. No. 3,705,907) were dissolved in 100 ml. pyridine. To this solution were added dropwise, while cooling to 0°-5° C., 6.5 g. (6.7 ml.) pivaloyl chloride. After an hour, the reaction mixture was poured on to ice and extracted with diethyl ether. The ethereal solution was successively washed with dilute sulfuric acid, aqueous sodium bicarbonate solution and water. After drying and treating with active charcoal, the solution was filtered and evaporated. The residue (13 g.; 82% of theory) crystallized upon triturating with diethyl ether/ligroin to give 4-(2,3-epoxypropoxy)-2-pivaloyloxymethyl-indole; m.p. 129°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152446
Source datasetuspto-grants-1979_05
ORD IDord-6292074dad134276a0a9e8699974bfe1
Source noteuspto-grants-1979_05