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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468282Generated: October 26, 2026

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

https://huagongshe.com/reaction/468282

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 mm 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 numberUS08623905B2
Source datasetuspto-grants-2014_01
ORD IDord-1ee44163c0d34ba2a7f76bb53257259a
Source noteuspto-grants-2014_01