HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385407Generated: October 29, 2026
1,3-Dibromopropane → Ethyl 1-(3-(cyclopropylmethoxy)-4-nitrophenyl)cyclobutanecarboxylate
https://huagongshe.com/reaction/385407
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)acetate | HCID 57995474 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 1-(3-(cyclopropylmethoxy)-4-nitrophenyl)cyclobutanecarboxylate | HCID 57995510 | 49% |
Reaction Steps
Ethyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)acetate (5 g, 17.9 mmol) was dissolved in 50 mL anhydrous DMF, NaH (60% wt. in oil, 1.43 g, 35.9 mmol) was added at 0° C. The reaction mixture was stirred for 0.5 h at 25° C. and 1,3-dibromopropane (1.91 mL, 17.9 mmol) was added drop wise at 0° C. The reaction mixture was stirred at 0° C. for 1 h and saturated NH4Cl solution (10 mL) was added. The reaction mixture was extracted with EtOAc (3×20 mL) and the combined organic phases were washed with water (3×20 mL) and brine (20 mL), dried over MgSO4, filtered and concentrated under reduced pressure to give ethyl 1-(3-(cyclopropylmethoxy)-4-nitrophenyl)cyclobutanecarboxylate (2.8 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367863B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-c31bcd5b69774bd5b2b31034a33bc54d |
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| Source note | uspto-grants-2013_02 |
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