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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748962Generated: October 30, 2026

Lawesson's reagent → HCID 86671704, compound

https://huagongshe.com/reaction/1748962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantPropionamide, N-(2-fluoren-yl)-2-methyl-HCID 148890—
SolventTolueneHCID 1140—
ProductHCID 86671704HCID 86671704196.3%

Reaction Conditions

Temperature130 °C

Reaction Steps

In a 500 mL three-neck flask were put 20 g (80 mmol) of N-(9H-fluoren-2-yl)isobutyramide, 16 g (40 mmol) of 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-disulfide (Lawesson's reagent), and 150 mL of toluene, and the mixture was heated and refluxed at 130° C. for 4 hours. After that, the precipitated solid was washed with toluene and subjected to suction filtration to give 21 g of a yellow solid of N-(9H-fluoren-2-yl)isobutyrthioamide in a yield of 100%. The synthesis scheme of Step 2 is shown in (c-2) below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09155158B2
Source datasetuspto-grants-2015_10
ORD IDord-ad2eb7eaae9b4d70926e462687d2aadc
Source noteuspto-grants-2015_10