HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710883Generated: October 30, 2026
Acetic Anhydride → 3-Acetaminobenzyl alcohol
https://huagongshe.com/reaction/1710883
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Aminobenzyl alcohol | HCID 80293 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Acetaminobenzyl alcohol | HCID 96639 | 74.1% |
Reaction Steps
To a solution of (3-aminophenyl)methanol (1.87 g, 14.7 mmol) in tetrahydrofuran (10 mL) was added triethylamine (7 mL, 73.5 mmol). The reaction was cooled down to 0° C., acetic anhydride (1.5 mL, 16 mmol) was added dropwise. The reaction was warmed to room temperature overnight. The reaction mixture was partitioned between ethyl acetate and H2O. The ethyl acetate layer was dried over MgSO4, concentrated, trituated with CH2Cl2 to yield N-(3-(hydroxymethyl)phenyl)acetamide as a yellow solid (1.8 g, 74%). HPLC retention time (Method C)=1.03 min. LC/MS (ESI) (M+H)+=166.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790745B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-acf3aa17ed994537a2900057ae80fb57 |
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| Source note | uspto-grants-2010_09 |
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