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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411257Generated: October 31, 2026

3-Methylbenzoic acid → HCID 70032842, compound

https://huagongshe.com/reaction/411257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylbenzoic acidHCID 7418—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 131723872HCID 131723872—
SolventDimethylformamideHCID 6228—
ProductHCID 70032842HCID 70032842—

Reaction Steps

3-Methylbenzoic acid (0.3 mmol) was treated with a 0.4 M solution of 1,1′-carbonyldiimidazole (CDI) (0.75 mL, 0.3 mmol) in DMF in a 4 mL vial. After mixing for 30 minutes, a 0.22 M solution of Example 187C (0.75 mL, 0.16 mol) in DMF was added to the vial. The mixture was stirred for 4 hours at room temperature and a 0.4 M solution of CDI (0.5 mL, 0.2 mmol)in DMF was added to the vial. After heating the mixture at 115° C. for 7 hours, the mixture was allowed to cool to room temperature and then was concentrated under reduced pressure. The residue was purified by preparative HPLC to provide the desired product. 1H NMR (CDCl3) δ1.50 (d, 3H), 2.35 (m, 2H), 2.45 (s, 3H), 3.05-3.60 (m, 6H), 3.80-4.25 (m, 6H), 5.05 (m, 1H), 6.80 (m, 2H), 7.00 (m, 1H), 7.08 (m, 1H), 7.40 (m, 2H), 7.50 (m, 1H), 7.60 (m, 1H), 8.00 (m, 2H), 8.05 (m, 1H); MS (APCI+) m/z 564 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559140B2
Source datasetuspto-grants-2003_05
ORD IDord-9a43095315b04882a05f9b37e7a8c888
Source noteuspto-grants-2003_05