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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465935Generated: November 2, 2026

Potassium tert-butoxide → HCID 67235046, compound

https://huagongshe.com/reaction/1465935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67233095HCID 67233095—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67235046HCID 67235046—

Reaction Conditions

Temperature-15 °C

Reaction Steps

5-Bromo-3-{[(2,4-dimethoxy-benzyl)-ethoxycarbonylmethyl-amino]-methyl}-thiophene-2-carboxylic acid ethyl ester (example 21.b, 7.0 g, 14.1 mmol) was dissolved in 140 mL of anhydrous THF and cooled to −15° C. in a brine dry ice bath. A solution of 30 mL of 1.0 M potassium tert-butoxide in UV was added slowly to cold solution, and the reaction mixture was stirred at −15° C. for 30 min. and then at room temperature for 2 hours. The reaction was quenched with 29 mL of 1N HCl, and 400 mL ammonium chloride, and extracted twice with 300 mL ethyl acetate. The organic fractions were washed with brine, dried over anhydrous sodium sulfate and concentrated to 5.67 g of a tan viscous oil: MS: (+) m/z 453.6, 455.5 (M+1, 79Br/81Br)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000006B2
Source datasetuspto-grants-2015_04
ORD IDord-ed1f9bd2f15348b49cdfdf368e300dce
Source noteuspto-grants-2015_04