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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723636Generated: October 30, 2026

tert-Butyl methyl ether → HCID 66795672, compound

https://huagongshe.com/reaction/723636

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 3-(4-aminophenyl)acrylateHCID 97826—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDichloromethaneHCID 6344—
ProductHCID 66795672HCID 66795672—

Reaction Steps

The acid from above (0.519 g, 2.0 mmol) was dissolved in DCM (10 mL). DIEA (1.39 mL, 8.0 mmol, 4 equivalents) was added, followed by ethyl 4-aminocinnamate (0.573 g, 3.0 mmol, 1.5 equivalent) and HATU (1.143 g, 3.0 mmol, 1.5 equivalents). The mixture was stirred at room temperature for 3 days. The reaction was poured into TBME (100 mL) and the solution washed successively with 10% aqueous citric acid (2×25 mL) and saturated aqueous NaHCO3 (25 mL), and dried over MgSO4. The solvent was removed under reduced pressure and the residue stirred with TFA (10 mL) for 30 min. Volatiles were then removed under reduced pressure and the residue was co-evaporated twice with hexane. The crude product was dissolved in TBME (60 mL) and the solution washed with 1N NaOH (2×25 mL). After drying (Na2SO4), volatiles were removed in vacuum to give the title compound as a light brown solid (0.500 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141574B2
Source datasetuspto-grants-2006_11
ORD IDord-40b8f62dddeb49eabda5055c73f2c27f
Source noteuspto-grants-2006_11