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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102247Generated: October 30, 2026

Triethylamine → HCID 67334794, compound

https://huagongshe.com/reaction/2102247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 68623162HCID 68623162—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67334794HCID 67334794—

Reaction Steps

To a solution of the intermediate from step F (100 mg, 0.225 mmol) in DCM (3 mL) was added triethyl amine (94 μl, 0.675 mmol) followed by trimethyl acetyl chloride (33.25 μL, 0.27 mmol). After 2 hours the reaction was diluted with DCM (10 mL) and washed with 1N HCl, saturated Na2CO3, dried over brine and concentrated in vacuo to give a colorless oil. This material was dissolved in THF (2 mL) and MeOH (1 mL) and 2N NaOH (2 mL) were added and the reaction left stirring at room temperature for 16 hours. The reaction was concentrated in vacuo. The residue was suspended in 1N HCl (until the pH was less then 2). The resulting suspension was extracted with EtOAc (3×), dried over anhydrous Na2SO4, filtered and concentrated in vacuo to give the title compound as a white solid. 1H NMR (DMSO, 500 MHz): δ 7.93(d, J=8.2 Hz, 2H), 7.81(d, J=1.8 Hz, 2H), 7.51(t, J=2.1 Hz, 1H), 7.26(d, J=8.3 Hz, 2H), 6.94(s, 1H), 5.54(s, 2H), 4.34(d, J=13.3 Hz, 2H), 3.0(m, 1H), 2.86(t, J=12.9 Hz, 2H), 2.51(t, J=1.6 Hz, 1H), 1.74 (d, J=1 Hz, 2H), 1.44 (dq, J=3.4, 12.8 Hz, 2H), 1.2(s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572922B2
Source datasetuspto-grants-2009_08
ORD IDord-300ddc322f364f618dba810ce9736555
Source noteuspto-grants-2009_08