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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78734Generated: October 28, 2026

Triethylamine → HCID 86704313, compound

https://huagongshe.com/reaction/78734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantIndolineHCID 10328—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant(2E,4S)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-2-hexenoic acidHCID 86704312—
SolventDichloromethaneHCID 6344—
ProductHCID 86704313HCID 8670431389%

Reaction Steps

A solution of 50 wt % ®T3P in EtOAc (22.00 mL, 37.0 mmol) was added dropwise via addition funnel to a solution of (2E,4S)-4-({[(1,1-dimethylethyl)oxy]carbonyl}-amino)-2-hexenoic acid (5.65 g, 24.64 mmol), 2,3-dihydro-1H-indole (2.76 mL, 24.64 mmol), and Et3N (11 mL, 79 mmol) in CH2Cl2 (90 mL) at 0° C. (bath temp). The ice bath was removed, and the reaction was stirred at RT. After 30 min, the reaction was quenched by dropwise addition of saturated aq. NaHCO3 (50 mL). The layers were separated, and the reaction was washed with 10% citric acid (1×50 mL). The organic layer was concentrated under a stream of nitrogen, and the residue was purified by flash column chromatography, giving 7.21 g (89%) of the title compound. LC-MS m/z 331 (M+H)+, 1.05 (ret time).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841463B2
Source datasetuspto-grants-2014_09
ORD IDord-0979e192fad94202b22a5e2006d53b1e
Source noteuspto-grants-2014_09