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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378169Generated: October 25, 2026

Hydrochloric Acid → (3-Bromo-5-iodophenyl)methanol

https://huagongshe.com/reaction/378169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantMethyl 3-bromo-5-iodobenzoateHCID 21942573—
SolventDichloromethaneHCID 6344—
Product(3-Bromo-5-iodophenyl)methanolHCID 1546737996.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To methyl 5-bromo-3-iodobenzoate (Step A above) (5.01 g, 0.015 mole) in anhydrous methylene chloride (100 mL) at -78° C., was added dropwise minutes, diisobutylaluminum hydride (5.50 mL, 0.03 mole). The mixture was stirred for 1 hour then allowed to warm to 0° C. The reaction solution was poured into 600 mL, chilled 3N HCl and extracted 3× with methylene chloride (150 mL). The organic layers were combined, dried over MgSO4 and concentrated under vacuum to yield 5-bromo-3-iodobenzyl alcohol (4.54 g) as a white solid. MP=110-112° C. MS and NMR were consistent with the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028223
Source datasetuspto-grants-2000_02
ORD IDord-7a3136ee0bb84c16864a250cede4929f
Source noteuspto-grants-2000_02