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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600913Generated: October 29, 2026

4-Methylmorpholine → HCID 57805756, compound

https://huagongshe.com/reaction/600913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57805891HCID 57805891—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57805756HCID 5780575692.2%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a stirred solution of (S)-3-((benzyloxy)carbonyl)-2-(1,3-dioxoisoindolin-2-yl)propanoic acid (compound 7-2, 6.07 mmol) in 30 mL of dry THF at −15° C. were successively added N-methylmorpholine (6.07 mmol), iso-butylchloroformate (6.07 mmol). After stirring for 5 min at −15° C., a solution of NaBH4 (689 mg, 18.21 mmol) in 2.73 mL of water were added at once. The reaction was stirred at −15° C. for 2 min, then hydrolyzed with water (30 mL). Extracted with EtOAc (×3), washed with water (×3), brine (×1), dried over sodium sulfate, filtered, concentrated. Purification by chromatography on silica gel column (hexane/EtOAc) to give 1.9 g of colorless oil, compound 7-3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902240B2
Source datasetuspto-grants-2011_03
ORD IDord-07532c46b64e4e34baeb3aa4ae9385a2
Source noteuspto-grants-2011_03