HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250869Generated: November 2, 2026
Lithium borohydride → (3-Benzyloxy-4-iodophenyl)methanol
https://huagongshe.com/reaction/250869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl 3-(benzyloxy)-4-iodobenzoate | HCID 57443321 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Benzyloxy-4-iodophenyl)methanol | HCID 45140291 | — |
Reaction Steps
1.18 g (54 mmol, 3 eq) of lithium borohydride are added to a solution of 6.9 g of methyl 3-benzyloxy-4-iodobenzoate in 30 ml of tetrahydrofuran. The reaction medium is heated at 60° C. for 12 hours and then hydrolyzed with ammonium chloride solution and extracted with ethyl acetate. The organic phases are combined and the solvents are evaporated off. 6.5 g of (3-benzyloxy-4-iodophenyl)methanol in oil form are used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863332B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-729da5f1eed4487da047b3d0a10cfb8a |
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| Source note | uspto-grants-2011_01 |
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