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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330255Generated: October 29, 2026

5-Bromonaphthalene-2-carboxylic acid → HCID 13477023, compound

https://huagongshe.com/reaction/330255

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromonaphthalene-2-carboxylic acidHCID 14960646—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13477023HCID 13477023—

Reaction Steps

To a stirred solution of 5-bromonaphthalene-2-carboxylic acid (10.04 g, 40 mmol) in dry THF (400 mL) cooled to 0° C. was added BH3 ·THF (54 mL, 54 mmol; 1.0M solution in THF) dropwise over 45 minutes. The resulting solution was stirred overnight while warming to room temperature. The excess BH3 was quenched by the addition of H2O (200 mL) at 0° C. and the volatiles were removed in vacuo. The aqueous residue was extracted with Et2O (2×250 mL) and the combined organic layers were dried (MgSO4) and concentrated in vacuo to give the title compound as a colorless liquid which solidified to a white solid upon standing (9.48 g, 100%). This material was of adequate purity to be used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895861
Source datasetuspto-grants-1990_01
ORD IDord-2beab8e882734413aa1b25f4914e2302
Source noteuspto-grants-1990_01