Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60776Generated: October 29, 2026

Sodium borohydride → HCID 89748270, compound

https://huagongshe.com/reaction/60776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-Benzyl-2-((tert-butoxycarbonylamino)methyl)-5-fluoropyridinium bromideHCID 89739413—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 89748270HCID 8974827062%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaBH4 (5.56 mmol, 0.21 g) was added to a solution of 1-benzyl-2-((tert-butoxycarbonylamino)methyl)-5-fluoropyridinium bromide (1.40 mmol, 0.60 g) in MeOH at 0° C. The resulting mixture was stirred at 0° C. for 40 min. An aliquot was checked by analytical HPLC and some of the starting material remained. Additional NaBH4 (5.56 mmol, 0.21 g) was added at 0° C. and the resulting mixture was stirred for extra 40 min. The reaction mixture was diluted with EtOAc and washed with brine. EtOAc layer was separated, dried with MgSO4 and concentrated in vacuo to give desired tert-butyl (1-benzyl-5-fluoro-1,2,3,4-tetrahydropyridin-2-yl)methylcarbamate in 62% yield which was used for next step without further purification. MS (ESI) 321 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440982B2
Source datasetuspto-grants-2016_09
ORD IDord-702c2305c8d94f92869c11bce1371cc2
Source noteuspto-grants-2016_09