HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375553Generated: October 25, 2026
1-Bromo-2-Chloroethane → 1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclopropane
https://huagongshe.com/reaction/375553
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Reactant | 1-(Carboethoxy)-1-(4-methoxybenzylthio)methane | HCID 10847644 | — |
| Reactant | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclopropane | HCID 22400217 | 21% |
Reaction Steps
Cool lithium hexamethyldisilazane (6 mL of a 1.0M solution tetrahydrofuran, 6.0 mmol) to -78° C. Add, by cannula transfer, a solution of 1-(carboethoxy)-1-(4-methoxybenzylthio)methane (1.36 g, 5.66 mmol) in tetrahydrofuran (10 mL). Stir for 45 minutes, add 1,3-dimethyl -3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) (0.73 mL, 6.0 mmol) followed by 1-bromo-2-chloroethane (050 mL, 6.0 mmol) and stir to room temperature overnight. Cool to -78° C., add lithium hexamethyldisilazane (6.0 mL, 6.0 mmol) and stir at room temperature for 24 hours. Quench with saturated ammonium chloride (5 mL) and partition between ethyl acetate (30 mL) and water (30 mL). Separate the organic phase, dry (Na2SO4) and evaporate the solvent in vacuo. Purify by chromatography (5:1 hexane/ethyl acetate to 2.5:1 hexane/ethyl acetate) to give 1-(carboethoxy)-1-(4-methoxybenzylthio)cyclopropane (317 mg, 21%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05486513 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-6fa1becc54914fbeb8ef2d6422006083 |
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| Source note | uspto-grants-1996_01 |
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