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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042418Generated: November 2, 2026

Formamide → HCID 70926266, compound

https://huagongshe.com/reaction/1042418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
Reactant(+-)-CashmeranHCID 92292—
ReactantHCID 70926894HCID 70926894—
SolventTolueneHCID 1140—
ProductHCID 70926266HCID 70926266—

Reaction Conditions

Temperature200 °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) and formamide (NH2CHO) (50 mL). The reaction mixture is heated to 200° C. and stirred for 24 hours. The crude mass is diluted with toluene (50 mL) and then washed once with aqueous sodium carbonate (10%, 100 mL) followed by twice with brine (30 mL). Toluene is recovered by roto-evaporation. The crude product is further purified with liquid chromatography (Biotage® system) and then crystallized. Product of a mixture of 6,6,7,8,8-pentamethyl-5,6,7,8-tetrahydro-4H-1-oxa-3-aza-as-indacene and 6,6,7,8,8-pentamethyl-5,6,7,8-tetrahydro-4H-indeno[4,5-d]oxazole (˜10 g) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557876B2
Source datasetuspto-grants-2013_10
ORD IDord-ca55f678340d4da187ed9b17765d55f6
Source noteuspto-grants-2013_10