HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289083Generated: October 31, 2026
1-Bromo-2-methylpropane → HCID 54419340, compound
https://huagongshe.com/reaction/1289083
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 54535325 | HCID 54535325 | — |
| Reactant | HCID 178418816 | HCID 178418816 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54419340 | HCID 54419340 | 98% |
Reaction Steps
A tetrahydrofuran solution of 2-methylpropylmagnesiumbromide prepared from 2.9 g of 2-methylpropylbromide, 0.47 g of magnesium and 20 ml of tetrahydrofuran was cooled to 10° C., a solution containing 1 g of 2-acetyl-3-t-butyloxycarbonylaminothiophene in 10 ml of tetrahydrofuran was dropwise added at 15° C. or less, and the mixture was stirred at room temperature for 2 hours. Thereafter a saturated aqueous ammonium chloride solution was dropwise added under cooling. The reaction mixture was extracted with ethyl acetate, washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium solfate. The solvent was distilled off under reduced pressure to obtain 1.2 g of the product. The yield was 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747518 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-201853f512e74500963d436256cb310d |
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| Source note | uspto-grants-1998_05 |
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