HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363667Generated: October 28, 2026
Ammonium Chloride → (2,3-Dihydro-1-benzofuran-7-yl)methanol
https://huagongshe.com/reaction/1363667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,3-Dihydro-1-benzofuran-7-carbaldehyde | HCID 2795018 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2,3-Dihydro-1-benzofuran-7-yl)methanol | HCID 2795020 | — |
Reaction Steps
2,3-Dihydro-benzofuran-7-carbaldehyde (1.50 g, 10.20 mmol) was dissolved in ether, then cooled to 0° C., NaBH4 (400 mg, 10.57 mmol) in MeOH (5.00 mL) was added. The resulting reaction mixture was stirred for 30 min, then saturated ammonium chloride was added. The mixture was extracted with ether, and the combined organic phases were washed with brine, then dried over magnesium sulfate and concentrated to afford the desired alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884244B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-3de0f6cb22b94ecfbc20de4fa8479d92 |
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| Source note | uspto-grants-2011_02 |
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