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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175327Generated: November 1, 2026

Sodium borohydride → HCID 58565346, compound

https://huagongshe.com/reaction/2175327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58565344HCID 58565344—
SolventMethanolHCID 887—
ProductHCID 58565346HCID 5856534692.6%

Reaction Steps

To a mixture of 1-[1-(3-fluorophenyl)-1H-indol-2-yl]ethanone (0.27 g, 1.1 mmol) in methanol (6 mL) was added sodium tetrahydroborate (41 mg, 1.1 mmol). The reaction was stirred at room temperature for 1 hour, quenched with water, and extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4 and concentrated to give title compound (0.26 g). The crude product was used directly in the next step. LCMS calculated for C16H13FN(M-OH)+: m/z=238.1. Found: 238.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062055B2
Source datasetuspto-grants-2015_06
ORD IDord-60821f8ad1fa49eeaea5332fca0ac192
Source noteuspto-grants-2015_06