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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252748Generated: November 2, 2026

Triphenylphosphine → HCID 14574967, compound

https://huagongshe.com/reaction/1252748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 14574965HCID 14574965—
CatalystBoranuide;copper(1+);triphenylphosphaneHCID 12406461—
SolventAcetoneHCID 180—
SolventBenzeneHCID 241—
ProductHCID 14574967HCID 1457496770%

Reaction Steps

By following the procedure employed in Preparation 1, E. and F., 3,3-(ethylenedioxy)glutaric acid mono benzyl ester prepared as described above in step A. (2.937 g, 10.48 mmole) was converted to the corresponding acid chloride with oxalyl chloride (3.0 ml, 34.39 mmole) in 30 ml of benzene. The acid chloride was reduced with bis(triphenylphosphine) copper (I) tetrahydroborate (6.32 g, 10.48 mmole) and triphenylphosphine (5.5 g, 20.97 mmole) in 50 ml of acetone. There was obtained 1.930 g, 70% yield of benzyl 3,3-(ethylenedioxy)-4-formylbutyrate, as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04745201
Source datasetuspto-grants-1988_05
ORD IDord-5f49ab529e7e457197156a0bd93db3b2
Source noteuspto-grants-1988_05