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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837391Generated: November 3, 2026

Phenol → 4,4-Diaminodiphenylmethane

https://huagongshe.com/reaction/1837391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantDiphenylmethane diisocyanateHCID 7570—
ReactantDiphenyl carbonateHCID 7597—
ReactantPhenyl carbamateHCID 69322—
ReactantPhenyl formateHCID 74626—
ReactantHCID 88047488HCID 88047488—
SolventFormic AcidHCID 284—
Product4,4-DiaminodiphenylmethaneHCID 757791.6%

Reaction Steps

The di-formamide of 4,4′-methylene-dianiline is prepared by the reaction of the diamine with 2.1 molar equivalents of formic acid, and removing the water byproduct by azeotropic distillation with toluene. Using the same apparatus as Example 1, but without the addition funnel, diphenyl carbonate (48.45 grams, 0.226 mole) and 4,4′-MDA-di-formamide (6.92 grams, 0.0272 mole), containing 0.21 grams of phenol, is heated to reflux at 38 mmHg. Reaction and phenol/phenyl formate distillation commences at a pot temperature of 155° C., and ceases 30 minutes later at a pot temperature of 195° C., 17 mmHg. IS/GC analysis of the condensate (10.55 grams) shows only phenyl formate, phenol and a trace of DPC. The pot material (43.97 grams) contains 3.02 grams of 4,4′-diphenylmethane diisocyanate (MDI) and 3.21 grams of MDI as the mono-phenol carbamate, a recovery of 0.0249 mole equivalents of MDI, equal to a 91.6% yield, based on di-formamide charged.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06781010B1
Source datasetuspto-grants-2004_08
ORD IDord-e815a674b88d4b5a8d8a339c841e6d21
Source noteuspto-grants-2004_08