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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098660Generated: October 30, 2026

Sodium borohydride → (1-Boc-6-fluoro-5-indazolyl)methanol

https://huagongshe.com/reaction/1098660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59490926HCID 59490926—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(1-Boc-6-fluoro-5-indazolyl)methanolHCID 5949088184.1%

Reaction Steps

A solution of tert-butyl 6-fluoro-5-formyl-1H-indazole-1-carboxylate (29E, 3.55 g, 13.4 mmol) in methanol (50.00 mL) was treated with NaBH4 (1.02 g, 26.9 mmol) at 0° C. and allowed to stir for 1 h. The reaction mixture was diluted with water and EtOAc (500 mL). The organic layer was separated and washed with aq. HCl (1M, 200 mL), aq. NaOH (1M, 200 mL) brine (200 mL) dried (MgSO4), filtered, concentrated in vacuo and residue was purified using chromatography (SiO2, EtOAc/hexanes) to provide tert-butyl 5-(hydroxymethyl)-6-fluoro-1H-indazole-1-carboxylate (29F, 3.00 g; Yield=83.9%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143305B2
Source datasetuspto-grants-2012_03
ORD IDord-2abe2bf6acc147c3b09af3833993ea40
Source noteuspto-grants-2012_03