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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051202Generated: October 31, 2026

Triethylamine → HCID 178447232, compound

https://huagongshe.com/reaction/1051202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 178418806HCID 178418806—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 178447232HCID 17844723276%

Reaction Steps

3-Aminopyrazole (9 g, 108 mmol) was dissolved in DCM (250 ml). Triethylamine (27 g, 262 mmol) was added in one portion. Pivaloyl chloride (30 g, 248 mmol) was added slowly at room temperature. After stirring at room temperature for 6 hours, the solvent was concentrated under reduced pressure to give a solid. The solid was dissolved in methanol (200 ml). Aqueous NaOH (2.5M, 120 ml) was added slowly and the mixture was stirred at room temperature for 30 minutes. The solvent was evaporated off under reduced pressure. The slurry was transferred into water (300 ml). The solid was filtrated and dried to give the title product (13.5 g) as a yellow solid, yield: 76%. 1H-NMR (400 MHz, d6-DMSO): δ 12.3 (s, 1H), 9.77 (s, 1H), 7.58 (s, 1H), 6.49 (s, 1H), 1.2 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388168B2
Source datasetuspto-grants-2016_07
ORD IDord-7e8c5d9564a748969cb126835af72816
Source noteuspto-grants-2016_07