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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856851Generated: November 3, 2026

Dimethylformamide → HCID 21224857, compound

https://huagongshe.com/reaction/1856851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 21224829HCID 21224829—
ReactantHCID 178418443HCID 178418443—
SolventDiisopropyl EtherHCID 7914—
ProductHCID 21224857HCID 21224857—

Reaction Steps

10 g of the product obtained in Stage 3 above is introduced into 200 ml of anhydrous tetrahydrofuran. 10 ml of ethyl magnesium bromide (3M solution in ethyl ether) is added and the reaction medium is left under agitation for 20 minutes at ambient temperature. Then an excess of anhydrous dimethylformamide is added. After 2 hours at ambient temperature, hydrolysis is carried out with 200 ml of 1N hydrochloric acid and extraction is carried out 3 times with 300 ml of ethyl acetate. The organic phase is washed with saturated sodium chloride then dried and evaporated to dryness. The residue obtained is impasted in isopropyl ether. In this way 7.6 g of expected product is obtained, which is used without purification for the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143774
Source datasetuspto-grants-2000_11
ORD IDord-2c6c6d3b3e4c440883187f8c521b9b73
Source noteuspto-grants-2000_11