HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60776Generated: October 29, 2026
Sodium borohydride → HCID 89748270, compound
https://huagongshe.com/reaction/60776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Benzyl-2-((tert-butoxycarbonylamino)methyl)-5-fluoropyridinium bromide | HCID 89739413 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 89748270 | HCID 89748270 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09440982B2 |
|---|
| Source dataset | uspto-grants-2016_09 |
|---|
| ORD ID | ord-702c2305c8d94f92869c11bce1371cc2 |
|---|
| Source note | uspto-grants-2016_09 |
|---|