HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464537Generated: October 31, 2026
Methyl iodide → 2,2-Dimethyl-1H-indene-1,3(2H)-dione
https://huagongshe.com/reaction/1464537
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,3-Indandione | HCID 11815 | — |
| Product | 2,2-Dimethyl-1H-indene-1,3(2H)-dione | HCID 599983 | — |
Reaction Steps
Preparations of compounds listed in the above Table I are given below for illustrative purposes. ##STR76## 20 g (0.137 moles) of indan-1,3-dione was added to 200 ml of acetonitrile. 26 ml (0.41 moles) of methyl iodide and 8 g of a KF-celite (1:1) mixture were then added to this mixture and the resulting red mixture stirred for 18 hours at 60° C. under a nitrogen atmosphere. After cooling, the precipitate was filtered off and washed with acetonitrile. The filtrate was then evaporated to dryness and the residue chromatographically purified using a silica column with hexane/ether (6:4) as the eluent. 10.5 g of 2,2-dimethyl-indan-1,3-dione was obtained with a melting point of 107° C. ##STR77##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05306587 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-f192a401675045538f8bab197f74ff61 |
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| Source note | uspto-grants-1994_04 |
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