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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362726Generated: November 1, 2026

Sodium borohydride → HCID 58513754, compound

https://huagongshe.com/reaction/2362726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58513752HCID 58513752—
SolventMethanolHCID 887—
ProductHCID 58513754HCID 58513754—

Reaction Steps

To an ambient solution of tert-butyl 3-(2-methoxy-2-oxoethoxy)-3-(thiazol-2-yl)pyrrolidine-1-carboxylate (2.05 g, 5.99 mmol) in methanol (29.9 ml) was added NaBH4 (0.680 g, 17.96 mmol). The reaction was stirred for 1 hour and was then quenched by the addition of water (20 mL) and ethyl acetate (20 mL). The layers were separated, and the aqueous layer was extracted with additional ethyl acetate (2×20 mL). The combined organic layers were dried with anhydrous Na2SO4, filtered, and concentrated under reduced pressure to give the title compound, which was used in the subsequent step without further purification. MS ESI(+) m/z 314.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691810B2
Source datasetuspto-grants-2014_04
ORD IDord-ae89f94dc63b492886827a92dc0e10be
Source noteuspto-grants-2014_04