HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453635Generated: October 30, 2026
Sulfuric Acid → 1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene
https://huagongshe.com/reaction/1453635
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Pentanone, 4-methyl-4-phenyl- | HCID 81898 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Indane | HCID 10326 | — |
| Product | 1,1,3,3-Tetramethyl-2,3-dihydro-1H-indene | HCID 14026682 | 85.5% |
Reaction Steps
Methyl magnesium bromide (3M solution in diethyl ether, 22.2 mL, 66.6 mmol) was added slowly to a solution of 4-methyl-4-phenyl-pentan-2-one (Compound 40, 7.8 g, 44.3 mmol) in 50 mL of tetrahydrofuran (THF) at 0° C. After stirring and warming to room temperature for 2 h, the mixture was quenched with water at 0° C., extracted with ethyl acetate (3×10 mL), washed with brine (1×10 mL), dried (MgSO4) and concentrated at reduced pressure to give a light yellow oil. The crude oil was then added slowly to 80% concentrated sulfuric acid at 0° C. and the resulting brown mixture was stirred at 0° C. for 1 h. The mixture was then slowly diluted with ice water, extracted with pentane (3×15 mL) and washed with brine (1×15 mL). After the extract was dried (MgSO4) and concentrated at reduced pressure, high-vacuum distillation of the residue afforded indan the title compound (3.3 g, 43% yield) as a colorless oil:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476673B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-c09853de39484a7b8163510a43951a6f |
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| Source note | uspto-grants-2009_01 |
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