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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707923Generated: October 30, 2026

Benzaldehyde → HCID 18960336, compound

https://huagongshe.com/reaction/1707923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTolueneHCID 1140—
ReactantHCID 18960345HCID 18960345—
SolventMethanolHCID 887—
SolventTrimethyl orthoformateHCID 9005—
ProductHCID 18960336HCID 18960336—

Reaction Steps

Three g (9 mmol) of 2,3-bis-tert.-butoxycarbonyloxy-benzaldehyde were dissolved at room temperature in 10 ml of methanol and 1.2 ml of trimethyl orthoformate. For complete dissolution of the benzaldehyde derivative, 1.5 ml of toluene were added. This was followed by the addition of 3.75 mg of RhCl3 [CH3C(CH2PPh2)3 ] as catalyst. The mixture was then stirred overnight at room temperature. The solvents were separated off by steam distillation and the oily residue was taken up in a little toluene. The undissolved rhodium catalyst was filtered off over a G-4 frit. After the toluene had been stripped off under reduced pressure, the product was dried in an oil pump vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356752
Source datasetuspto-grants-1994_10
ORD IDord-530afe2a2df14a12a854afdb63032089
Source noteuspto-grants-1994_10