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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626942Generated: November 2, 2026

Trifluoroacetic acid → HCID 1515311, compound

https://huagongshe.com/reaction/626942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl 2-butynoateHCID 78043—
ReactantBenzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
SolventDichloromethaneHCID 6344—
ProductHCID 1515311HCID 151531127%

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzyl(methoxymethyl)[(trimethylsilyl)methyl]amine (10.78 mL, 42.12 mmol) and ethyl but-2-ynoate (5.89 mL, 50.54 mmol) were stirred in DCM (500 mL) at 0° C. under nitrogen, then trifluoroacetic acid (161 μL, 2.11 mmol) was added dropwise. The reaction mixture stirred at 0° C. for 20 minutes, then the ice bath was removed and the solution was allowed to warm to room temperature. The solution was stirred at room temperature overnight. The mixture was concentrated and purified by FCC, eluting with 0-70% EtOAc in heptane, to afford the title compound (2.76 g, 27%). δH (500 MHz, DMSO-d6) 7.38-7.32 (m, 4H), 7.30-7.23 (m, 1H), 4.13 (q, J 7.1 Hz, 2H), 3.75 (s, 2H), 3.60-3.51 (m, 4H), 2.05 (s, 3H), 1.22 (t, J 7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309243B2
Source datasetuspto-grants-2016_04
ORD IDord-04707362a582490c9ddbed181c4969e2
Source noteuspto-grants-2016_04