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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968931Generated: October 30, 2026

Tetrahydro-4H-pyran-4-one → HCID 59016635, compound

https://huagongshe.com/reaction/968931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
Reactant3-Methoxy-2-methylbenzohydrazideHCID 45091273—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 59016635HCID 5901663583.5%

Reaction Steps

3-methoxy-2-methyl-benzoic acid hydrazide (4.14 g, 23 mmol) was suspended in a mixture of 80 mL of ether, 40 mL of CH2Cl2 and 2 drops of acetic acid. A solution of tetrahydro-pyran-4-one (2.3 g, 23 mmol) in 20 mL of CH2Cl2 and 2-3 mL of methanol were added, and the mixture was refluxed for 10 minutes. The reaction mixture was allowed to cool and was concentrated to about 80 mL. Pentane (100 mL) was added, resulting in the formation of a precipitate. The suspension was chilled in a freezer and filtered to yield 5.04 g of 3-methoxy-2-methyl-benzoic acid (tetrahydro-pyran-4-ylidene)-hydrazide as a tan, flocculent, semi-crystalline material. 1H NMR (300 MHz, CDCl3)δ(ppm): 7.2 (t, 1H), 6.98 (d, 1H), 6.95 (d, 1H), 3.9 (t, 2H), 3.86 (s, 3H), 3.8 (t, 2H), 2.65 (t, 2H), 2.42 (t, 2H), 2.35 (s, 3); Rf=0.15 (3:1 ethyl acetate:hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304162B2
Source datasetuspto-grants-2007_12
ORD IDord-025e8494c4564f40940d4e3cc5b959eb
Source noteuspto-grants-2007_12