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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930329Generated: November 3, 2026

Trichloroethanol → HCID 69036822, compound

https://huagongshe.com/reaction/1930329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroethanolHCID 8259—
Reactant1,4-DioxaneHCID 31275—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 57507619HCID 57507619—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 69036822HCID 6903682273%

Reaction Steps

To a stirring solution of 3-tert-butyl-1-(3-fluorophenyl)-1H-pyrazole-5-carboxylic acid (0.26 g, 0.60 mmol) and TEA (0.13 ml, 0.90 mmol) in 1,4-dioxane (9 ml) was added DPPA (0.16 ml, 0.75 mmol), After stirring for 30 min at RT, 2,2,2-trichloroethanol (0.58 ml, 6.0 mmol) was added and the reaction was heated at 100° C. for 2 h. The reaction mixture was diluted with brine (10 ml) and extracted with EtOAc (3×20 ml). The combined organic phases were washed with 5% citric acid (10 ml), satd. NaHCO3 (10 ml), dried (MgSO4), filtered and evaporated. The crude product was purified by chromatography to afforded 2,2,2-trichloroethyl 3-tert-butyl-1-(3-fluorophenyl)-1H-pyrazol-5-ylcarbamate (0.180 g, 73% yield) as colorless oil. MS (ESI) m/z: 410(M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188113B2
Source datasetuspto-grants-2012_05
ORD IDord-84d714f6ebcb4b45b9c2040e63b50750
Source noteuspto-grants-2012_05