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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358345Generated: October 26, 2026

Sodium borohydride → isopropyl 2(S)-(tert-butoxycarbonylamino)-5-hydroxypentanoate

https://huagongshe.com/reaction/2358345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantIsopropyl 1-(tert-butoxycarbonyl)pyrrolidin-5-one-2(s)carboxylateHCID 21080141—
ReactantEthyl acetate hexaneHCID 21226206—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Productisopropyl 2(S)-(tert-butoxycarbonylamino)-5-hydroxypentanoateHCID 2108014264%

Reaction Steps

To a solution of isopropyl 1-(tert-butoxycarbonyl)pyrrolidin-5-one-2(S)-carboxylate (product of step 26B, 49.5 g, 183 mmol) in methanol (300 mL) was added sodium borohydride (10.0 g, 263 mmol) in ˜1 g portions over 1.5 hours. The reaction was stirred under nitrogen for another 10 minutes. It was diluted with water, extracted with ether, combined organic fractions washed with saturated aqueous NaCl, dried (MgSO4) and evaporated to give a light yellow oil. Flash chromatography (silica gel, 20-30% ethyl acetate/hexane) gave 31.8 g (64%) of isopropyl 2(S)-(tert-butoxycarbonylamino)-5-hydroxypentanoate as a colorless syrup:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763584B2
Source datasetuspto-grants-2010_07
ORD IDord-fcc2a6f19a034f1389f6ffe30e2dfef0
Source noteuspto-grants-2010_07