HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852778Generated: October 27, 2026
Ethyl 1-bromocyclobutanecarboxylate → HCID 178517981, compound
https://huagongshe.com/reaction/852778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 1-bromocyclobutanecarboxylate | HCID 97595 | — |
| Reactant | N-Cycloheptylthiourea | HCID 13433274 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 178517981 | HCID 178517981 | — |
Reaction Steps
A mixture of 1-cycloheptylthiourea (0.255 g, 1.48 mmol) and ethyl 1-bromocyclobutanecarboxylate (0.25 mL, 1.48 mmol, Aldrich) in N,N-diisopropylethylamine (0.5 mL) and ethanol (1.0 mL) was heated in a sealed tube in a microwave oven (Emrys Optimizer from Personal Chemistry) at 155° C. for 2 h, then at 170° C. for 1.5 h. After removing the low-boiling solvents in vacuo, the residue was partitioned between EtOAc and water. The organic portion was separated, washed with brine, and conc. in vacuo. The residue was purified by flash column chromatography (0 to 35% of EtOAc in hexanes) to give the title compound as a tan solid. MS m/z: 253.2 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253196B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-0b7708e015c947018d4e37eb80c582d2 |
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| Source note | uspto-grants-2007_08 |
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