HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253540Generated: October 30, 2026
HCID 59598472, compound → (R)-tert-butyl 2-(5-methoxypentanoyl)morpholine-4-carboxylate
https://huagongshe.com/reaction/253540
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59598472 | HCID 59598472 | — |
| Reactant | HCID 178495008 | HCID 178495008 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-tert-butyl 2-(5-methoxypentanoyl)morpholine-4-carboxylate | HCID 59598474 | 93% |
Reaction Steps
To a solution of (R)-tert-butyl 2-(methoxy(methyl)carbamoyl)morpholine-4-carboxylate (1.37 g, 5.0 mmol) in THF (10 mL) at −20° C., there was added (4-methoxybutyl)magnesium chloride in THF (1.47 M, 10.2 mL, 15.0 mmol) dropwise such that the temperature remained below −20° C. After addition, the resulting solution was warmed to rt, and quenched with 1 N aq HCl (10 mL). The organic layer was separated, and the aqueous layer was extracted with ether (3×5 mL). The combined organic layers were washed with satd aq NaHCO3 (10 mL) and brine (5 mL), and dried over Na2SO4. The solvent was then removed in vacuo to give (R)-tert-butyl 2-(5-methoxypentanoyl)morpholine-4-carboxylate (1.41 g, 93%), which was used for the next step without purification; MS m/s 324 (M+Na+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872028B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-36657eaff8514535827fb593f8f22f5b |
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| Source note | uspto-grants-2011_01 |
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