HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263497Generated: October 31, 2026
4-Methylmorpholine → Boc-Asp(O-cHex) Man(4-MBzl)
https://huagongshe.com/reaction/263497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Boc-Asp(OcHx)-OH | HCID 7009416 | — |
| Reactant | Man(4-MBzl) | HCID 131720063 | — |
| Catalyst | Isobutyl chloroformate | HCID 62365 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-Asp(O-cHex) Man(4-MBzl) | HCID 131720065 | 92.1% |
Reaction Steps
To a cold solution of Boc-Asp(O-cHex), (31.5 g, 100 mmol) in THF (500 mL) and N-methylmorpholine (13.1 g, 120 mmol), isobutylchloroformate (15.6 mL, 1.2 mmol) was added dropwise. The reaction mixture was stirred for a few minutes and 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, the reaction mixture was filtered 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), 10% aqueous NaHCO3 (1×400 mL), water (1×400 mL) and saturated salt solution (1×300 mL). The solution was dried (anhydrous K2CO3), filtered and concentrated to yield the titled compound (53 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05643872 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-926680f640c445d68e90af716e3fe069 |
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| Source note | uspto-grants-1997_07 |
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