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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755161Generated: November 1, 2026

Formaldehyde → 4-{[(4-tert-Butyl-phenyl)-(4-iodo-phenylcarbamoyl)-methyl]-methyl-amino}-benzoic Acid Tert-butyl Ester

https://huagongshe.com/reaction/1755161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantEthyl AcetateHCID 8857—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-{[(4-tert-Butyl-phenyl)-(4-iodo-phenylcarbamoyl)-methyl]-amino}-benzoic Acid Tert-butyl EsterHCID 67486559—
SolventAcetic AcidHCID 176—
Product4-{[(4-tert-Butyl-phenyl)-(4-iodo-phenylcarbamoyl)-methyl]-methyl-amino}-benzoic Acid Tert-butyl EsterHCID 67486343105.5%

Reaction Steps

4-{[(4-tert-Butyl-phenyl)-(4-iodo-phenylcarbamoyl)-methyl]-amino}-benzoic acid tert-butyl ester (110 mg, 0.19 mmol) was dissolved in 2 mL of HOAc. paraformaldehyde (51 mg, 0.57 mmol) and sodium cyano-borohydride (36 mg, 0.57 mmol) were then added and heated to 40 C for 1 h. Cooled to RT, EtOAc (20 mL) was added and extracted water (20 mL). The organic layer was washed again with water (20 mL), dried over sodium sulfate, filtered and the organic layer was removed under reduced pressure to give a white solid (120 mg, 100%). 1H NMR showed the compound to be very clean and sufficient for the following step. LCMS (M+1=599.4)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169201B2
Source datasetuspto-grants-2015_10
ORD IDord-0d7737b6e4c0441a9e2c48411aeec3a3
Source noteuspto-grants-2015_10