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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883715Generated: November 1, 2026

Tributylamine → HCID 69859806, compound

https://huagongshe.com/reaction/1883715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantEthyl trans-crotonateHCID 429065—
ReactantHCID 12683815HCID 12683815—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 69859806HCID 69859806—

Reaction Steps

A mixture of 4-acetylamino-7-bromoindane (2.8 g, prepared according to the method of A. Courtin, Helv. Chim. Acta 1980, 63(8), pages 2280-2286), ethyl crotonate (2.51 g), palladium diacetate (150 mg), tri-ortho-tolyl phosphine (450 mg) and tributylamine (10 mL) in dimethylformamide (30 mL) was stirred at 120° C. for 4 hours under a nitrogen atmosphere. The mixture was cooled to room temperature, then allowed to stand for 48 hours, then partitioned between ethyl acetate (500 mL) and aqueous hydrochloric acid (300 mL, 1M). The organic phase was washed with 5% aqueous sodium bicarbonate (150 mL) and then filtered. The clear yellow filtrate was dried over sodium sulfate then evaporated. The residue was subjected to normal phase HPLC on silica under gradient elution conditions using ethyl acetate, heptane and methanol mixtures (from 20:80:1 to 90/10/1, v/v/v) to give the title compound (1.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762199B2
Source datasetuspto-grants-2004_07
ORD IDord-c251122a0417482ea9848f96c421eeba
Source noteuspto-grants-2004_07