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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033862Generated: October 31, 2026

Methanol → HCID 131718220, compound

https://huagongshe.com/reaction/1033862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 129713539HCID 129713539—
CatalystPalladiumHCID 23938—
SolventDichloromethaneHCID 6344—
ProductHCID 131718220HCID 13171822096.2%

Reaction Steps

A 2-l three-necked round bottomed flask was fitted with a condenser and a dropping funnel to add solid material. To this flask was added anhydrous dichloromethane (850-ml) and methanol (420-ml). To this organic solution was added 10% palladium on carbon (14.0 g), the mixture was stirred under an argon blanket, and then cooled in an ice bath. Sodium borohydride (4.0 g, mol) was added in small portions over about 30-min. Next the dinitrotetraphenylporphyrin (7.0 g, 0.01 mol) and solid sodium borohydride (14.0 g) were added in small portions over about 60-min. The reaction mixture was stirred under argon for 30 min. The reaction mixture was filtered through a layer of CELITE® (diatomateous earth of Johns Manville, Denver, Colo.) in a Buchner funnel and washed repeatedly with dichloromethane. The solvent was completely removed under reduced pressure to produce a crude residue. The residue was redissolved in dry dichloromethane to separate insoluble CELITE®, and filtered. The solvent was removed under reduced pressure and dried to produce a purified residue (6.2 g). This residue was flash chromatographed over silica using dichloromethane as eluent. The product obtained (0.6 g, 9.6% yield) was free of impurities. See FIG. 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312896
Source datasetuspto-grants-1994_05
ORD IDord-ed9940f023114b65b908dbb815c41afb
Source noteuspto-grants-1994_05