Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736618Generated: October 29, 2026

Triethylamine → HCID 54280683, compound

https://huagongshe.com/reaction/1736618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Pentadienoic acid, methyl esterHCID 73688—
Reactant2-Bromo-N-(tert-butoxycarbonyl)benzylamineHCID 7018300—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 54280683HCID 5428068353.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3.0 g (10.5 mmol) of 1-(tert-butoxycarbonylaminomethyl)-2-bromobenzene, 4.5 ml (32.3 mmol) of triethylamine, 1.82 ml (15.7 mmol) of methyl 2,4-pentadienoate and 0.2 g (0.28 mmol) of bis (triphenylphosphine) palladium (II) chloride was sealed in a heavy-walled Pyrex, Teflon screw-capped flask and heated at 100° C. for 40 hours. After being cooled to 25° C. the reaction mixture was diluted with 150 ml of water and 50 ml of ether. The aqueous phase was extracted with ether. The combined ether extracts were washed with water and brine, dried (Na2SO4) and concentrated. The residue was chromatographed on a silica gel column that was eluted with a 5 to 10% gradient of ethyl acetate in hexane to give 1.6 g (53.3%) of colorless needles, mp 96°-97.5° C. after recrystallization from 1:3 ether:hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541286
Source datasetuspto-grants-1996_07
ORD IDord-e884642c698549d48599dd3198ed55c2
Source noteuspto-grants-1996_07