Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392849Generated: October 28, 2026

Iodine → 1,1'-(Diazomethylene)bis(benzene)

https://huagongshe.com/reaction/2392849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantDiphenylmethylidenehydrazineHCID 79304—
SolventDichloromethaneHCID 6344—
Solvent1,1,3,3-TetramethylguanidineHCID 66460—
Product1,1'-(Diazomethylene)bis(benzene)HCID 61230—

Reaction Steps

To a solution of benzophenone hydrazone (11.3 g) in CH2Cl2 (58 mL) is added a 1% w/v solution of iodine in CH2Cl2 (2.3 mL) and 1,1,3,3-tetramethylguanidine (7.29 g). 3-Chloroperoxybenzoic acid (11 g) is then added in small portions at room temperature. The solvent is removed in vacuo to provide diphenyl diazomethane. A solution of diphenyl diazomethane (10 g) in EtOAc (22 mL) is then added to a cooled (5° C.) solution of Compound 12 (9.7 g) in THF (170 mL) and EtOAc (170 mL). The mixture is stirred until completion whereupon it is evaporated to dryness in vacuo. THF (73 mL) is added and the insolubles are filtered off. The filtrate is evaporated in vacuo until crystals begin to form. EtOAc (73 mL) is then added and the mixture is stirred for 1.5 hours at 0°-5° C. The resulting solid is filtered to provide Compound 13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05801242
Source datasetuspto-grants-1998_09
ORD IDord-e85128c2dc7545668ef65ee316381d38
Source noteuspto-grants-1998_09