HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481333Generated: October 31, 2026
Methanol → 2-(Aminomethyl)-3,5-dichlorobenzenemethanol
https://huagongshe.com/reaction/1481333
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3,5-Dichloro-2-cyanobenzyl acetate | HCID 89704760 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Aminomethyl)-3,5-dichlorobenzenemethanol | HCID 89704696 | — |
Reaction Steps
To a solution of 3,5-dichloro-2-cyanobenzyl acetate (11.7 mmol) in 50 mL THF was added a solution of BH3 (50 mmol, 1M in THF). The reaction mixture was heated to 75° C. for 7 h and then cooled to 0° C. Water was added followed by MeOH and the mixture was concentrated. The residue was taken up in water and EtOAc, acidified with 1N HCl solution and extracted with DCM. The aqueous phase was then basified with 1M NaOH solution and extracted with DCM. The combined organic layers were dried over MgSO4 and concentrated in vacuo. Purification with CC using DCM/Et3N (99/1) to DCM/MeOH/Et3N (90/10/1) gives the desired compound as pinkish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409917B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-edb1037ba85146e69218818efdd5d281 |
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| Source note | uspto-grants-2016_08 |
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