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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456392Generated: October 29, 2026

Water → tert-Butyl 2-(hydroxymethyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/456392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium borohydrideHCID 4148881—
Reactant4-tert-Butyl 2-methyl morpholine-2,4-dicarboxylateHCID 58817474—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 2-(hydroxymethyl)morpholine-4-carboxylateHCID 5201202—

Reaction Steps

The crude product from step (i) (62.6 mmol) was dissolved in dry tetrahydrofuran (THF) (100 ml) and added dropwise at 0° C. to a suspension of lithium borohydride (2.50 g, 115 mmol) in dry THF (100 ml). The mixture was allowed to attain room temperature over night. Water (10 ml) was added and after stirring for 1 h the mixture was concentrated. The residue was partitioned between ethyl acetate and water. The organic phase was washed with 0.5 M hydrochloric acid, saturated sodium hydrogen carbonate and water. Drying over magnesium sulfate and concentration gave the title compound as a crude product (13.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186718B2
Source datasetuspto-grants-2007_03
ORD IDord-868578121e3c4fc391be969e260f58bb
Source noteuspto-grants-2007_03