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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530646Generated: November 3, 2026

Sodium borohydride → HCID 118276758, compound

https://huagongshe.com/reaction/530646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 118276731HCID 118276731—
SolventMethanolHCID 887—
ProductHCID 118276758HCID 11827675896%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-2-(6-Methoxy-pyridine-3-carbonyl)-morpholine-4-carboxylic acid tert-butyl ester (305 mg, 0.95 mmol) was dissolved in methanol (5 mL) and cooled to 0° C. Sodium borohydride (36 mg, 0.95 mmol) was added and the resulting reaction mixture was stirred for 2 h at room temperature before pouring onto NaHCO3 and extracting 3 times with ethyl acetate. The combined organic phase was washed with brine, dried over MgSO4, filtered and concentrated to afford (S)-2-[hydroxy-(6-methoxy-pyridin-3-yl)-methyl]-morpholine-4-carboxylic acid tert-butyl ester (295 mg, 96%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353096B2
Source datasetuspto-grants-2016_05
ORD IDord-6737af898e854597a5e3e29198f324a7
Source noteuspto-grants-2016_05