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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638443Generated: October 26, 2026

Formaldehyde → 4-Hydroxybutyraldehyde 2-hydroxytetrahydrofuran

https://huagongshe.com/reaction/1638443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSulfuric AcidHCID 1118—
Reactant1,4-ButanediolHCID 8064—
ReactantSodium HydroxideHCID 14798—
Reactant2-Methyl-1,4-butanediolHCID 18053—
Reactant2,3-DihydrofuranHCID 70934—
ReactantTetrahydro-2-hydroxyfuranHCID 93002—
Reactant4-HydroxybutanalHCID 93093—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventWaterHCID 962—
Product4-Hydroxybutyraldehyde 2-hydroxytetrahydrofuranHCID 86743497—

Reaction Steps

The 4-hydroxybutyraldehyde/2-hydroxytetrahydrofuran was prepared by adding 20 parts of 2,3-dihydrofuran to 10 parts of 2% H2SO4 over about 20 minutes, keeping the temperature at 35° with cooling. The mixture was then neutralized with 30% NaOH. The organic portion of the resulting homogeneous product was a 2:1 mixture of 4-hydroxybutyraldehyde and its cyclic hemiacetal, 2-hydroxytetrahydrofuran. Thirty parts of that mixture were mixed with 10 parts of water, 4.3 parts of 37% aqueous formaldehyde, 0.53 parts of 30% NaOH, and 2 parts of Raney nickel. Hydrogenation was then carried out at 27,576 kPa (gauge) hydrogen at 150° for 2 hours in a shaker tube. The organic portion of the resulting product consisted mainly of 1,4-butanediol and 2-methyl-1,4-butanediol, in a ratio of 55:45. There were also some unidentified higher boilers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04879420
Source datasetuspto-grants-1989_11
ORD IDord-adb34929297e49359d06c1c1b69d311e
Source noteuspto-grants-1989_11