HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876193Generated: October 30, 2026
1,1,3,3,5,5,5-Heptamethyltrisiloxane → HCID 178504321, compound
https://huagongshe.com/reaction/876193
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1,3,3,5,5,5-Heptamethyltrisiloxane | HCID 76170 | — |
| Reactant | HCID 178457715 | HCID 178457715 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178504321 | HCID 178504321 | 75.3% |
Reaction Steps
1.03 g (2.19 mmol) of perylene tetracarboxylic acid bis(allylimide) (compound (6), m=1, n=1) and 1.53 g (6.87 mmol) of 1,1,1,3,3,5,5-heptamethyl trisiloxane were dissolved in 100 ml of toluene, and 20 μl of a Karstedt catalyst (2 mol/l solution in xylene) was thereafter added thereto, which was then refluxed for 5 hours. The reaction solution thus obtained was then cooled and filtered, and the toluene was distilled off from a filtrate. The crude product thus obtained was purified by silica gel column chromatography (eluent: dichloromethane→dichloromethane-ethyl acetate (50:1)). The resultant crude product was dissolved in dichloromethane and re-precipitated with methanol. Thus, 1.51 g (1.65 mmol) of a red powder was obtained as an intended compound (1-1). A yield of the compound (1-1) was 75.3%. Values obtained by instrumental analysis of the compound (1-1) are shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987044B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-70af0e72bb454d04b2d336c6e7e5aaaa |
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| Source note | uspto-grants-2015_03 |
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