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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911700Generated: November 1, 2026

2,5-Dichlorothiophene-3-carboxylic acid → 219765-84-1

https://huagongshe.com/reaction/1911700

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dichlorothiophene-3-carboxylic acidHCID 225438—
Reactant3-(Bromomethyl)-2,5-dichlorothiopheneHCID 23434082—
SolventTetrahydrofuranHCID 8028—
Product219765-84-1HCID 22388014—

Reaction Steps

3-bromomethyl-2,5-dichloro-thiophene: Borane-THF complex (6.009 mL, 6.01 mmol) was added dropwise into a THF (5 mL) solution of 2,5-dichlorothiophene-3-carboxylic acid (296 mg, 1.502 mmol). The resultant solution was stirred at rt under argon overnight. The reaction was quenched with dilute HCl (12 mL) and stirred at rt for 1 h. The reaction was diluted with water and extracted with EtOAc (2×20 mL), washed with NaOH solution and brine, dried (Na2SO4), filtered and evaporated to provide (2,5-dichloro-thiophen-3-yl)-methanol, which was purified by flash chromatography. LCMS m/z 183.2 (M+H)+. To a solution of this intermediate (215 mg, 1.175 mmol) in DCM (7 mL) was added PBr3 (0.144 mL, 1.527 mmol) via syringe. The reaction mixture was stirred at rt under argon for 15 min, then quenched with water (18 mL) and stirred at rt for 1 h. The aqueous layer was extracted with DCM (2×10 ml) and the combined organic layers were dried (Na2SO4), filtered and concentrated yielding 103A (250 mg). 1HNMR (400 MHz, CD3OD) δ: 4.47 (s, 2H), 7.02 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604056B2
Source datasetuspto-grants-2013_12
ORD IDord-ac82ce1102ea45e5b87b96b64fb346ba
Source noteuspto-grants-2013_12