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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543006Generated: October 30, 2026

4-Methylmorpholine → HCID 86741435, compound

https://huagongshe.com/reaction/543006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantN-MethylisobutylamineHCID 12249—
ReactantIsobutyl chloroformateHCID 62365—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86741436HCID 86741436—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86741435HCID 86741435—

Reaction Conditions

Temperature-10 °C

Reaction Steps

N-Methylmorpholine (0.028 ml.) and isobutyl chloroformate (0.038 ml.) were successively added to a stirred solution of 11-(3-benzyloxy-17β-hydroxyoestra-1,3,5(10)-trien-7α-yl)undec-10-enoic acid (0.109 g.) in tetrahydrofuran (3 ml.) which was cooled to -10° C. The mixture was stirred at -10° C. for 30 minutes, N-methylisobutylamine (0.05 ml.) was added and the mixture was stirred at laboratory temperature for 2 hours. Saturated aqueous sodium bicarbonate solution (5 ml.) was added and the mixture was extracted 3 times with methylene chloride (10 ml. each time). The combined extracts were washed with water (2 ml.), dried and evaporated to dryness, and there was thus obtained as oily residue N-isobutyl-N-methyl-11-(3-benzyloxy-17β-hydroxyoestra-1,3,5(10)-trien-7αyl)undec-10-enamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659516
Source datasetuspto-grants-1987_04
ORD IDord-bc561b1dd35145eb80764f989f5ed38b
Source noteuspto-grants-1987_04