HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78734Generated: October 28, 2026
Triethylamine → HCID 86704313, compound
https://huagongshe.com/reaction/78734
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Indoline | HCID 10328 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | (2E,4S)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-2-hexenoic acid | HCID 86704312 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86704313 | HCID 86704313 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841463B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0979e192fad94202b22a5e2006d53b1e |
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| Source note | uspto-grants-2014_09 |
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