HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663600Generated: October 30, 2026
Ammonium Chloride → 5-Methyl-2-pyrazinemethanol
https://huagongshe.com/reaction/1663600
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 5-Methyl-2-pyrazinecarboxylic acid | HCID 122831 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-Methyl-2-pyrazinemethanol | HCID 580061 | 66% |
Reaction Steps
To a solution of 5-methyl-2-pyrazinecarboxylic acid (1.0 g) in tetrahydrofuran (10 mL) was added triethylamine (1.1 mL) and isobutyl chloroformate (1.0 mL), and the mixture was stirred at 0° C. for 30 minutes. To the reaction mixture was added sodium borohydride (603 mg) and methanol (5 mL) at −78° C. After stirring, to the mixture was added aqueous ammonium chloride and the mixture was extracted with ethyl acetate. The organic layer was separated and concentrated in vacuo. The resultant crude product was purified by a column chromatography on silica gel (solvent; chloroform/methanol=90:10) to give 5-methylpyrazin-2-ylmethyl alcohol (592 mg, yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034949B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-e8edbcfa7fc04615a046d12bcfbe221d |
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| Source note | uspto-grants-2011_10 |
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