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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355400Generated: November 1, 2026

Tert-butyl 2-(methoxy(methyl)carbamoyl)morpholine-4-carboxylate → HCID 57449676, compound

https://huagongshe.com/reaction/2355400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-(methoxy(methyl)carbamoyl)morpholine-4-carboxylateHCID 57449675—
ReactantHCID 178495008HCID 178495008—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57449676HCID 5744967693%

Reaction Steps

A stirred solution of (±)-tert-butyl 2-(methoxy(methyl)carbamoyl)morpholine-4-carboxylate (1.73 g, 6.4 mmol) in dry THF (40 mL) was cooled in an ice-salt bath and 1.34 M 4-methoxybutylmagnesium chloride in THF (10 mL, 1.34 mmol) was added dropwise over 3 min. The cooling bath was allowed to expire and the mixture was stirred at rt for 6 h, poured into ice cold 3% aq HCl (100 mL) and extracted with ether (2×100 mL). The combined ether extracts were washed with satd aq NaHCO3 (35 mL), dried over MgSO4 and concentrated to afford (±)-tert-butyl 2-(5-methoxypentanoyl)morpholine-4-carboxylate (1.78 g, 93%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-e6f728ee77034f0b901f0e96e8f9f4ac
Source noteuspto-grants-2010_07