HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748962Generated: October 30, 2026
Lawesson's reagent → HCID 86671704, compound
https://huagongshe.com/reaction/1748962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | Propionamide, N-(2-fluoren-yl)-2-methyl- | HCID 148890 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86671704 | HCID 86671704 | 196.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09155158B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-ad2eb7eaae9b4d70926e462687d2aadc |
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| Source note | uspto-grants-2015_10 |
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