HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065791Generated: November 2, 2026
Trichloroisocyanuric Acid → Methyl 1-formylcyclopropane-1-carboxylate
https://huagongshe.com/reaction/2065791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichloroisocyanuric Acid | HCID 6909 | — |
| Reactant | Methyl 1-(hydroxymethyl)cyclopropane-1-carboxylate | HCID 22934721 | — |
| Catalyst | Tempo | HCID 2724126 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 1-formylcyclopropane-1-carboxylate | HCID 53415969 | 120.5% |
Reaction Steps
Methyl 1-(hydroxymethyl)cyclopropanecarboxylate (16.0 g, 123.07 mmol) is dissolved in dichloromethane (320 mL) and the mixture is cooled to −5° C. Trichloroisocyanuric acid (29.1 g, 125.5 mmol) is added portionwise followed by the addition of TEMPO (1.9 g, 12.3 mmol). The reaction mixture is stirred at −5° C. for 20 min, allowed to warm to RT, and stirred for 20 min. The mixture is filtered through a pad of CELITE® and diluted with dichloromethane (500 mL). The solution is washed with saturated Na2CO3 (300 mL), 1 N HCl (300 mL), brine (300 mL), and saturated ammonium chloride (3×200 mL). The organic portion is dried over MgSO4, filtered, and concentrated under reduced pressure to obtain 19 g of the title compound, still containing dichloromethane (theoretical 15.75 g). The material is used as is in the next reaction. 1H NMR (400 MHz, CDCl3); δ 1.7-1.6 (m, 4H), 3.81 (s, 3H), 10.38 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288548B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-f2f32ee37baa43828d37d34f880d40da |
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| Source note | uspto-grants-2012_10 |
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