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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862056Generated: October 31, 2026

Sodium borohydride → Benzenemethanol, 5-bromo-2-(methoxymethoxy)-

https://huagongshe.com/reaction/862056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-Bromo-2-(methoxymethoxy)benzaldehydeHCID 19701626—
SolventMethanolHCID 887—
ProductBenzenemethanol, 5-bromo-2-(methoxymethoxy)-HCID 54142346100%

Reaction Steps

To a solution of 5-bromo-2-methoxymethoxybenzaldehyde (5.00 g) in methanol (50 ml) was added, at 0° C., sodium borohydride (0.46 g). The mixture was stirred for 30 minutes at the same temperature, which was then concentrated. To the concentrate was added ethyl acetate, and the mixture was washed with an aqueous solution of potassium hydrogensulfate and a saturated aqueous saline solution, successively. The organic layer was dried (anhydrous magnesium sulfate), which was then concentrated to leave 5-bromo-2-methoxymethoxybenzyl alcohol (5.04 g) as a pale yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716971
Source datasetuspto-grants-1998_02
ORD IDord-0a810795ea7145fd8dc67a46d3fa7d98
Source noteuspto-grants-1998_02