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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914773Generated: November 1, 2026

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

https://huagongshe.com/reaction/1914773

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 stirred 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 resulting residue was purified using chromatography (SiO2, EtOAc/hexanes) to yield 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 numberUS08614229B2
Source datasetuspto-grants-2013_12
ORD IDord-02e48e656a1f4188a2636d4363fd43a2
Source noteuspto-grants-2013_12