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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991648Generated: October 30, 2026

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

https://huagongshe.com/reaction/1991648

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 numberUS07645789B2
Source datasetuspto-grants-2010_01
ORD IDord-0b7f2426f9f14410a774679dcc76c4c5
Source noteuspto-grants-2010_01