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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204986Generated: October 31, 2026

Sodium hydride → (S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)butoxy)acetate

https://huagongshe.com/reaction/2204986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactanttert-butyl N-[(2S)-1-hydroxybutan-2-yl]carbamateHCID 11263954—
SolventTetrahydrofuranHCID 8028—
Product(S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)butoxy)acetateHCID 86678281—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (S)-tert-butyl 1-hydroxybutan-2-ylcarbamate (1 eq, from the previous step) in THF (0.23 M) at 0° C. was added portionwise 60% wt NaH (2 eq). The reaction was stirred at 0° C. for 30 minutes, and then a solution of tert-butyl 2-bromoacetate (1 eq) in THF (0.12 M) was added dropwise. The reaction was warmed to room temperature and stirred for 1 hour. The reaction was quenched slowly with saturated aqueous NH4Cl solution and diluted with ether. The organic layer was washed with water, brine, dried over anhydrous MgSO4, and concentrated en vaccuo. The crude mixture was purified by flash chromatography on a COMBIFLASH® system (ISCO) using a gradient of 0-40% ethyl acetate in hexanes to give the product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365506B2
Source datasetuspto-grants-2016_06
ORD IDord-05e68fc0d85a4d13aa9b1024a6e93039
Source noteuspto-grants-2016_06