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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72777Generated: October 29, 2026

Ethyl Acetate → HCID 85256537, compound

https://huagongshe.com/reaction/72777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantCbz-DL-ValinolHCID 14036742—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 85256537HCID 85256537—

Reaction Steps

To 11.0 g (0.0464 mole) of benzyl N-[1-(hydroxymethyl)-2-methyl-propyl]carbamate in dioxane (100 mL) cooled to 0° C. was added diphenylphosphoryl azide 10.99 mL (1.1 eq) followed by the addition of DBU 8.32 mL (1.2 eq). The contents were allowed to warm to room temperature and stirred for 16 hrs. After the addition of ethyl acetate (300 mL) and water (100 mL), the organic layer was separated and then washed with satd. NaHCO3 (100 mL). The organic layer was then dried (magnesium sulfate) and then concentrated under vacuum. To this intermediate in DMSO (100 mL) was added sodium azide 7.54 g and the contents then heated to 90 degrees for 2 hrs. After addition of ethyl acetate and water the layers were separated. The organic layer was dried with magnesium sulfate followed by concentration under vacuum to afford an oil that was columned using hexane/ethyl acetate (0-70%) to afford benzyl N-[1-(azidomethyl)-2-methyl-propyl]carbamate 6.9 g as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829012B2
Source datasetuspto-grants-2014_09
ORD IDord-4604cb0e626742c0a03f156580b389d2
Source noteuspto-grants-2014_09