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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569587Generated: October 29, 2026

Acetone → HCID 13067815, compound

https://huagongshe.com/reaction/569587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantAmmoniaHCID 222—
ReactantHydrogen SulfideHCID 402—
Reactant2-bromoheptanalHCID 10910384—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 13067815HCID 13067815—

Reaction Conditions

Temperature-10 °C

Reaction Steps

The procedure of M. Thiel, F. Asinger, K. Schmiedel, (Liebigs Ann. Chem. 611, 121 (1958)) was employed. To a methanol solution (3 liters) containing sodium methoxide (216.7 g, 4.01 mole) at -10° C. was added hydrogen sulfide (~1 lb) until the solution was saturated. To this solution was added dropwise over a 2 hour period 2-bromoheptaldehyde (775 g, 4.01 mol). The temperature of the reaction was maintained at about -10° C. after the addition, acetone (734 g, 12.6 mole) was added over a 10 minute period and the solution was stirred for an additional 20 minutes at about -10° C. at which time ammonia was added over a period of 1.5 hours. The solution was then poured into water (4 liters) and extracted with ether (4×1 liter). The combined etheral extracts were washed with brine (1×1 liter), dried over magnesium suflate and concentrated in vacuo to afford after distillation (70°-80°/1.5 mm) 549 g (74%) of 2,2-dimethyl-5-pentyl-3-thiazoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732988
Source datasetuspto-grants-1988_03
ORD IDord-86a9a48ccff94f33a9e1bb64232a3277
Source noteuspto-grants-1988_03