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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613615Generated: October 30, 2026

N-Formylmorpholine → HCID 15322096, compound

https://huagongshe.com/reaction/1613615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FormylmorpholineHCID 20417—
Reactant7-Bromo-2,3,4,5-tetrahydro-1-benzoxepin-5-olHCID 19774223—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15322096HCID 15322096105.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

254 ml (0.6 mole) of a 1.7 molar solution of tert.-butyllithium in n-pentane is slowly added dropwise under argon to a stirred solution of 48.6 g (0.2 mole) of 7-bromo-5-hydroxy-2,3,4,5-tetrahydro-1-benzoxepin in 550 ml of absolute THF at -90° C. to -100° C. The mixture is subsequently stirred at -78° C. for 1 hour and then, at this temperature, a solution of 24 ml (0.24 mole) of N-formylmorpholine in 180 ml of absolute THF is added dropwise while stirring vigorously. The mixture is stirred at -78° C. for 1 hour and subsequently allowed to warm to 0° C., and is diluted with diethyl ether and hydrolyzed with ice-water. After extraction several times with diethyl ether, the combined organic extracts are washed with water and saturated brine and dried over sodium sulfate, and the solvent is stripped off in vacuo. 40.7 g of yellowish oil are obtained and reacted further without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194442
Source datasetuspto-grants-1993_03
ORD IDord-d5a944520e0e42d0afacac9095d10382
Source noteuspto-grants-1993_03