Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518315Generated: October 27, 2026

Sodium borohydride → HCID 178499108, compound

https://huagongshe.com/reaction/1518315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178499107HCID 178499107—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178499108HCID 17849910889%

Reaction Conditions

Temperature70 °C

Reaction Steps

To compound 45C (2.08 g, 3.42 mmol) in MeOH (50 mL) and THF (20 mL) was added NaBH4 (0.259 g, 6.83 mmol). The reaction mixture was heated at 70° C. for 2 hours. The solvent was removed, and the residue was partitioned between EtOAc and water. The organic layer was isolated, and the aqueous layer was extracted with additional EtOAc. The combined organic layers were washed with brine, dried over MgSO4, and concentrated under reduced pressure. The crude material was purified by column chromatography on silica gel eluting with 1:1/hexanes:EtOAc to provide 1.86 g of the desired product: 1H NMR (DMSO-d6): δ 8.24-8.26 (m, 1H), 7.94 (d, J=7.67 Hz, 1H), 7.70 (d, J=8.20 Hz, 1H), 7.52-7.56 (m, 1H), 7.34-7.42 (m, 3H), 6.00 (s, 2H), 5.77 (t, J=5.52 Hz, 1H), 5.13 (s, 2H), 4.83 (d, J=5.52 Hz, 2H), 3.67-3.75 (m, 7H), 3.03 (t, J=5.98 Hz, 2H), 0.87-0.91 (m, 2H), −0.18 (s, 9H). MS (ESI(+)): m/z 611 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232273B2
Source datasetuspto-grants-2012_07
ORD IDord-daae09617a3047fca59d8342e4feb8b7
Source noteuspto-grants-2012_07