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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | tert-butyl N-[(2S)-1-hydroxybutan-2-yl]carbamate | HCID 11263954 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)butoxy)acetate | HCID 86678281 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365506B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-05e68fc0d85a4d13aa9b1024a6e93039 |
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| Source note | uspto-grants-2016_06 |
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