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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665722Generated: October 30, 2026

Sodium borohydride → (7-Fluoro-benzo[1,3]dioxol-5-yl)-methanol

https://huagongshe.com/reaction/1665722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant7-Fluorobenzo[d][1,3]dioxole-5-carbaldehydeHCID 59129153—
SolventMethanolHCID 887—
Product(7-Fluoro-benzo[1,3]dioxol-5-yl)-methanolHCID 59129331100%

Reaction Steps

To a solution of 7-fluoro-benzo[1,3]dioxole-5-carbaldehyde (0.80 g, 4.7 mmol) in MeOH (50 mL) was added NaBH4 (0.36 g, 9.4 mmol) in portions at 0° C. The mixture was stirred at this temperature for 30 min and was then concentrated to dryness. The residue was dissolved in EtOAc. The EtOAc layer was washed with water, dried over Na2SO4 and concentrated to dryness to afford (7-fluoro-benzo[1,3]dioxol-5-yl)-methanol (0.80 g, 98%), which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039491B2
Source datasetuspto-grants-2011_10
ORD IDord-4ceae08163e947b1b2c67b03d67a47fd
Source noteuspto-grants-2011_10