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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235102Generated: October 25, 2026

3,4-Dibromothiophene → HCID 10536833, compound

https://huagongshe.com/reaction/235102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DibromothiopheneHCID 18452—
ReactantN-Methoxy-N-methylpropionamideHCID 11344007—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 10536833HCID 1053683338.3%

Reaction Steps

A solution of 3,4-dibromothiophene (6.0 g, 24.8 mmol) in 10 mL of ether was cooled to -78° C. and trated with n-butyllithium (9.92 mL, 2.5M solution in hexanes, 24.8 mmol). While holding the temperature at -78° C., the reaction was stirred for 15 minutes, then 2.9 g (24.8 mmol) of N-methyl-N-methoxypropionamide was added and the reaction was stirred for 1 hour. The reaction was quenched with satd NH4Cl, and the mixture was diluted with ether. The ether layer was separated, washed with water and brine, dried over MgSO4 and concentrated. The residue was triturated with hexanes, and the mixture was filtered. The solvent was removed to give 2.08 g of a tan solid. MS 236, 238 (M+NH4)+. NMR (CDCl3) δ:7.99 (d, J=3 Hz, 1H), 7.32 (d, J=3 Hz, 1H), 2.98 (q, J=7 Hz, 2H), 1.21 (t, J=7 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597832
Source datasetuspto-grants-1997_01
ORD IDord-a348106b0b6d43e3a45bb6ec8506f1c4
Source noteuspto-grants-1997_01