Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361357Generated: October 26, 2026

Morpholine → 4-[(4-Bromothien-2-YL)methyl]morpholine

https://huagongshe.com/reaction/361357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product4-[(4-Bromothien-2-YL)methyl]morpholineHCID 78349750.6%

Reaction Steps

Sodium cyanoborohydride (2 g) was added portionwise to a stirred mixture of 4-bromo-2-thiophenecarbaldehyde (4.78 g), morpholine (2.1 g), glacial acetic acid (1.8 g) and ethanol (125 ml). The mixture was stirred at ambient temperature for 1 hour. The mixture was poured into a saturated aqueous sodium bicarbonate solution and extracted with methylene chloride. The organic phase was washed with brine and evaporated. The resultant oil was partitioned between a dilute (10%) aqueous hydrochloric acid solution and methylene chloride. The aqueous phase was basified by the addition of a saturated aqueous sodium bicarbonate solution and extracted with methylene chloride. The organic extract was dried (MgSO4) and evaporated to give 4-bromo-2-morpholinomethylthiophene (3.2 g);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866572
Source datasetuspto-grants-1999_02
ORD IDord-a14cb0c8039c46fc939b661a2cbf9c76
Source noteuspto-grants-1999_02