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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59598472HCID 59598472—
ReactantHCID 178495008HCID 178495008—
SolventTetrahydrofuranHCID 8028—
Product(R)-tert-butyl 2-(5-methoxypentanoyl)morpholine-4-carboxylateHCID 5959847493%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872028B2
Source datasetuspto-grants-2011_01
ORD IDord-36657eaff8514535827fb593f8f22f5b
Source noteuspto-grants-2011_01