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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709098Generated: October 30, 2026

Hydrochloric Acid → 5-(3-Bromopropyl)thiophene-2-carboxylic acid

https://huagongshe.com/reaction/709098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
Reactant2-Thiophenecarboxylic acidHCID 10700—
Reactant2,2-DibromopropaneHCID 11658—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product5-(3-Bromopropyl)thiophene-2-carboxylic acidHCID 53984314123.5%

Reaction Steps

To a solution consisting of thienoic acid (10 g, 78 mmol) in THF (150 mL) at −78° C. was added an LDA solution (85 mL, 170 mmol, 2 M in heptanes/THF/ethylbenzene, Sigma-Aldrich) dropwise over 20 minutes, and the reaction mixture was stirred 40 minutes. To the reaction mixture was then added dibromopropane (23.8 g, 117 mmol) in one portion, and the reaction mixture was allowed to warm to room temperature and was stirred for 3 days. To the reaction mixture was added 50 mL each of a saturated aqueous solution of ammonium chloride, a saturated aqueous solution of sodium chloride, and 6 N HCl. The organic material was extracted with ethyl acetate and the organic layer was dried over sodium sulfate, filtered, and concentrated to afford the title compound as a yellow oil (24.0 g). The product was used without further purification; TLC Rf 0.5 (solvent system: 30:70:1 v/v ethyl acetate-hexanes-acetic acid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180116B2
Source datasetuspto-grants-2015_11
ORD IDord-e1d2a0a2c0de448fb8859f49133bcd0e
Source noteuspto-grants-2015_11