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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451867Generated: October 29, 2026

Methanol → (S)-methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoate

https://huagongshe.com/reaction/451867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethyl SulfideHCID 1068—
Reactant(S)-2-((tert-butoxycarbonyl)amino)-5-methoxy-5-oxopentanoic acidHCID 7018756—
SolventTetrahydrofuranHCID 8028—
Product(S)-methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoateHCID 1110766749%

Reaction Steps

To a solution (S)-2-(tert-butoxycarbonylamino)-5-methoxy-5-oxopentanoic acid (26.1 g, 0.1 mol) in THF (500 mL), BH3.Me2S (80 mL, 0.8 mmol) was added dropwise at −78° C., then stirred at rt for 3 hrs. The reaction was stopped by careful addition of methanol. After evaporation and three distillations of methanol, the residue was dissolved in EtOAc, washed with 1 M NaHCO3, and brine. (S)-methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoate (12 g, yield 49%) was obtained as an oil that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-7c10b6e8df794ab78bcc16b9d584b0d9
Source noteuspto-grants-2013_07