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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371262Generated: October 31, 2026

Glyoxylic Acid → 4-{[(4-tert-Butyl-phenyl)-carboxy-methyl]-amino}-benzoic Acid Tert-butyl Ester

https://huagongshe.com/reaction/2371262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlyoxylic AcidHCID 760—
ReactantBenzoic acid, 4-amino-, 1,1-dimethylethyl esterHCID 233272—
ReactantTert-butylphenylboronic acidHCID 66584345—
SolventDichloromethaneHCID 6344—
Product4-{[(4-tert-Butyl-phenyl)-carboxy-methyl]-amino}-benzoic Acid Tert-butyl EsterHCID 67486232189.7%

Reaction Steps

In a 100 mL round bottom flask, t-butyl phenyl boronic acid (850 mg, 4.4 mmol), glyoxylic acid (404 mg, 4.4 mmol) and 4-Amino-benzoic acid tert-butyl ester (780 mg, 4.4 mmol) were dissolved in 25 mL of dichloromethane and allowed to stir at RT. After 30 min the reaction turned cloudy, but was allowed to stir an additional 2 h. Upon completion, the reaction was quenched with 20 mL water and the organic layer was separated, dried over sodium sulfate and filtered. The solvent was removed under reduced pressure to give 1.6 g (95%) of a light yellow powder. 1H NMR (CDCl3): δ 1.29 (9H, s), 1.55 (9H, s), 5.17 (1H, s), 6.57 (2H, d, J=8.4 Hz), 7.39 (4H, s), 7.78 (2H, d, J=8.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710236B2
Source datasetuspto-grants-2014_04
ORD IDord-bd4664df229944e2ab300156d982f669
Source noteuspto-grants-2014_04