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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643835Generated: November 1, 2026

Ozone → Dimethyl 5-(benzyloxy)-4-(2-oxoethyl)isophthalate

https://huagongshe.com/reaction/1643835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantDimethyl 4-allyl-5-(benzyloxy)isophthalateHCID 15281704—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductDimethyl 5-(benzyloxy)-4-(2-oxoethyl)isophthalateHCID 5956009698%

Reaction Steps

A solution of dimethyl 4-allyl-5-(benzyloxy)isophthalate (3.5 g, 10.28 mmol) in CH2Cl2 and methanol was cooled to −78° C. and treated with ozone until the solution appeared blue (20 min). Nitrogen was bubbled through the solution until the blue color dissipated. Dimethylsulfide (1.0 mL) was added and the cold-bath was removed allowing the reaction mixture to warm to room temperature overnight. Concentration of the solution under vacuum provided an oil which was purified by column chromatography on silica gel eluted with 10-30% EtOAc in hexanes to afford the aldehyde (3.0g, 98%) as a white solid. 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 3.90 (s, 3 H) 3.95 (s, 3 H) 4.29 (s, 2 H) 5.14 (s, 2 H) 7.31-7.56 (m, 5 H) 7.81 (d, J=1.32 Hz, 1 H) 8.29 (d, J=1.51 Hz, 1 H) 9.75 (s, 1 H); MS (ESI, pos): 343.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-faf6fbb8390f4fb6bb7ecd5cb7d642c9
Source noteuspto-grants-2012_02