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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934851Generated: November 1, 2026

6-Methyl-5-hepten-2-one → HCID 11263723, compound

https://huagongshe.com/reaction/1934851

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methyl-5-hepten-2-oneHCID 9862—
ReactantKeteneHCID 10038—
ReactantDiketeneHCID 12661—
CatalystHexamethylenetetramineHCID 4101—
CatalystBoron trifluoride etherateHCID 8000—
SolventNitrogenHCID 947—
SolventDichloromethaneHCID 6344—
ProductHCID 11263723HCID 1126372380.9%

Reaction Conditions

Temperature-19 °C

Reaction Steps

128.8 g (1.0 mol) of 6-methyl-5-hepten-2-one were dissolved in 516 g of dichloromethane in an N2 atmosphere. The solution was cooled to −19° C. 0.71 g of boron trifluoride etherate (0.5 mol % relative to 6-methyl-5-hepten-2-one) were then added and ketene gas was metered in over a period of 4 h. The temperature ranged between −12° C. and −14° C. The ketene gas was drawn directly from a diketene cracker: approx. 1.25 mol of ketene were generated from 55 ml of diketene and used. The solution was stirred overnight at −15° C., during which time an N2 stream was passed through the solution to remove excess ketene. Finally, 350 mg (2.5 mmol) of urotropine were added, the solution stirred again for 30 minutes and heated to 0° C. The solvent was then evaporated off at 15 mbar and 20° C. The crude product was obtained in the form of an orange solution. Distillation by way of a thin-film evaporator at 1-2 mbar and with an overhead temperature of 88° C. yielded 136 g (80.9%) of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384242B1
Source datasetuspto-grants-2002_05
ORD IDord-2bdc4044ed334acda7ce26c1e3c989d9
Source noteuspto-grants-2002_05