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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088022Generated: October 31, 2026

Tetrahydrofuran → HCID 22164489, compound

https://huagongshe.com/reaction/1088022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 14495344HCID 14495344—
ProductHCID 22164489HCID 2216448987%

Reaction Steps

A 10 1 magnetic lift stirred autoclave is charged with 1,015 g of 2,3,3-trimethoxyprop-1-ene together with 3,000 g of tetrahydrofuran and 500 mg of Rh2 (COD)2Cl2 as hydroformylation catalyst. The oxo reaction is carried out under a pressure of 500 bar (CO/H2 =1:1) at 40° C. for 6 hours, at 60° C./550 bar for another 6 hours and at 80° C./600 bar for a further 6 hours. According to gas chromatography, this way of carrying out the reaction gives a conversion of 94%. The desired compound 3,4,4-trimethoxybutanal (bp=135° C./110 mbar) is obtained in the yield of 87% following fraction-ation. Preparation of methyl 2-methoxyacrylate

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960954
Source datasetuspto-grants-1990_10
ORD IDord-d980a0fee8394500b686459609a61b05
Source noteuspto-grants-1990_10