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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912072Generated: October 31, 2026

Triethylethylenediamine → HCID 71114713, compound

https://huagongshe.com/reaction/1912072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylethylenediamineHCID 66040—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantSodium hexamethyidisilazaneHCID 45051731—
ReactantHCID 71114729HCID 71114729—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 71114713HCID 71114713—

Reaction Steps

A solution of (R)-4-benzyl-3-(5-benzyloxypentanoyl)oxazolidin-2-one (132 g) in tetrahydrofuran (660 mL) was added dropwise to a mixture of sodium hexamethyldisilazane (1.9 M in tetrahydrofuran) (702 mL) and tetrahydrofuran (660 mL) at −78° C. The reaction temperature was rose to −40° C. To the mixture was added dropwise tert-butyl bromoacetate (85 mL) at −78° C. The reaction temperature was rose to −36° C. To the mixture was added dropwise N,N,N′-triethylethylenediamine (33 mL) at ice temperature. And then, to the mixture were added water (530 mL) and hexane (660 mL). The aqueous layer was removed, and the organic layer was washed with aqueous 20 w/v % citric acid (660 mL×3), water (660 mL), saturated aqueous sodium bicarbonate (660 mL) and brine (660 mL), then dried over magnesium sulfate. The magnesium sulfate was filtered off and the filtrate was concentrated in vacuo to give the title compound (196 g) as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604069B2
Source datasetuspto-grants-2013_12
ORD IDord-7b99c2805d0145119d7d679cf144b258
Source noteuspto-grants-2013_12