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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438838Generated: November 2, 2026

Benzaldehyde → HCID 68119580, compound

https://huagongshe.com/reaction/1438838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 23050531HCID 23050531—
SolventIsopropanolHCID 3776—
ProductHCID 68119580HCID 68119580—

Reaction Conditions

Temperature0 °C

Reaction Steps

21.4 g of 4-amino-6-sec.-butyl-3-methylthio-1,2,4-triazin-5(4H)-one and 11.0 ml of benzaldehyde, dissolved in 50 ml of isopropanol, were briefly heated to the reflux temperature after adding 0.1 g of p-toluenesulfonic acid. On cooling to 0° C, 23.2 g of crude product crystallized out and were purified further by dissolving in 200 ml of boiling toluene. A small amount of a high-melting by-product crystallized out at 0° C and was filtered off and discarded. On concentration on a rotary evaporator, the mother liquor left 21.1 g (70%) of a pale oil which crystallized after trituration with a little methanol. The pure 4-benzylideneamino-6-sec.-butyl-3-methylthio-1,2,4-triazine-5 (4H)-one melted at 73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04057417
Source datasetuspto-grants-1977_11
ORD IDord-25fd7b8e4b9844cfb99183d53529aa68
Source noteuspto-grants-1977_11