HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473239Generated: October 29, 2026
Aluminium lithium hydride → 3-Aminomethyl-5-fluoromethylbenzylalcohol
https://huagongshe.com/reaction/473239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 3-azidomethyl-5-fluoromethylbenzoate | HCID 86671517 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Aminomethyl-5-fluoromethylbenzylalcohol | HCID 67253401 | 48% |
Reaction Steps
Methyl 3-azidomethyl-5-fluoromethylbenzoate (35) (476 mg, 2.13 mmol) was dissolved in THF (21.3 mL). The air was evacuated from the reaction system, and then Ar was charged therein. In another recovery flask filled with Ar, LiAlH4 (408 mg, 10.7 mmol) was placed. To this was added THF (21.3 mL) with ice-cooling to give a suspension. To the suspension was added dropwise the solution of the compound (35), and stirred for 2 hours at 0° C. TLC was used to confirm there was no starting material in the mixture. Then, the reaction was quenched with MeOH (10 mL). The mixture was filtered through cerite to remove metals. The filtrate was evaporated under reduced pressure. The residue was purified by neutral silica gel column chromatography (hexane:EtOAc=1:1, then EtOAc:MeOH=2:1) to isolate 3-aminomethyl-5-fluoromethylbenzylalcohol (38) (172 mg, 48%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633304B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-4dfb9da26e904d4fb5444bc8adfc1575 |
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| Source note | uspto-grants-2014_01 |
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