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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263501Generated: October 27, 2026

4-Methylmorpholine → Boc-Asp(O-cHex) Man(4-MBzl)

https://huagongshe.com/reaction/263501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBoc-Asp(OcHx)-OHHCID 7009416—
ReactantMan(4-MBzl)HCID 131720063—
CatalystIsobutyl chloroformateHCID 62365—
SolventTetrahydrofuranHCID 8028—
ProductBoc-Asp(O-cHex) Man(4-MBzl)HCID 13172006592.1%

Reaction Steps

To a cold solution of Boc-Asp(O-cHex) (31.5 g, 100 mmol) and N-methylmorpholine (13.1 g, 120 mmol) in THF (500 mL), isobutylchloroformate (15.6 mL, 1.2 mmol) was added dropwise. The reaction mixture was stirred for a few minutes, then a solution of Man(4-MBzl) (22.0 g, 96 mmol) in THF (500 mL) was added. The reaction mixture was allowed to warm to room temperature and stirred for 18 h. Upon completion of the reaction (monitored by TLC), the amine sand the filtered off and the filtrate was concentrated to dryness. The residue was dissolved in ethyl acetate (500 mL) and washed successively with 5% aqueous citric acid (3×150 mL), water (1×400 mL), aqueous NaHCO3 (1×300 mL), water (1×400 mL) and saturated salt solution (1×30 mL). The organic solvent was dried (anhydrous K2CO3), filtered and concentrated to yield the title product (53 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643872
Source datasetuspto-grants-1997_07
ORD IDord-8f1bfa25f2a246b5b287515bfd29d179
Source noteuspto-grants-1997_07