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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042420Generated: November 1, 2026

(+-)-Cashmeran → HCID 70926877, compound

https://huagongshe.com/reaction/1042420

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-CashmeranHCID 92292—
ReactantThioacetamideHCID 2723949—
ReactantHCID 70926894HCID 70926894—
SolventDiglymeHCID 8150—
ProductHCID 70926877HCID 70926877—

Reaction Conditions

Temperature130 °C

Reaction Steps

1,1,2,3,3-Pentamethyl-2,3,6,7-tetrahydro-1H-indene-4,5-dione is first prepared with 1,1,2,3,3-pentamethyl-1,2,3,5,6,7-hexahydro-inden-4-one (Cashmeran®) (commercially available at IFF) via oxidation with (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl (TEMPO) (prepared as described by Barton in Tetrahedron Letters, 1984, 25(6), pages: 603-606). A 100 mL reaction flask is charged with 1,1,2,3,3-pentamethyl-2,3,6,7-tetrahydro-1H-indene-4,5-dione (10 g, 0.04 mol), thioacetamide (CH3CSNH2) (3.5 g, 0.04 mol), and diglyme (50 mL). The reaction mixture is heated to 130° C. and stirred for 24 hours. The crude mass is washed once with aqueous sodium carbonate (10%, 100 mL) followed by twice with brine (30 mL). Diglyme is recovered by roto-evaporation. The crude product is further purified with liquid chromatography (Biotage® system) and then crystallized. Product 2,6,6,7,8,8-hexamethyl-5,6,7,8-tetrahydro-4H-3-thia-1-aza-as-indacene (˜10 g) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557876B2
Source datasetuspto-grants-2013_10
ORD IDord-2f1cc0ecfa82411a9e46f9f1e7cdcb35
Source noteuspto-grants-2013_10