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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528013Generated: November 2, 2026

Pyridine → Isopropyl 5-(2-bromoethyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/1528013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
ReactantIsopropyl 5-(2-hydroxyethyl)thiophene-2-carboxylateHCID 57487060—
SolventDichloromethaneHCID 6344—
ProductIsopropyl 5-(2-bromoethyl)thiophene-2-carboxylateHCID 5748706173%

Reaction Steps

Bromine (1.74 mL, 33.9 mmol) was added slowly to a solution of triphenylphosphine (8.9 g, 33.9 mmol) in CH2Cl2 (65 mL) at −40° C. After 1 h at −40° C., a solution of the alcohol from step 1 (6.6 g, 30.8 mmol) and pyridine (2.5 mL, 30.9 mmol) in CH2Cl2 (65 mL) was added via cannula. The mixture was allowed to warm to room temperature and was stirred overnight. The reaction was concentrated in vacuo to a brown slurry. The mixture was triturated with hexanes (150 mL) and stirred vigorously. The solids were removed by filtration and the filtrate was concentrated in vacuo to afford 6.2 g (73%) of isopropyl 5-(2-bromoethyl)thiophene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090584B2
Source datasetuspto-grants-2015_07
ORD IDord-de89cbe687de44b08f3719e45270e3e2
Source noteuspto-grants-2015_07