---
title: "Grignard reagent + CO₂ → carboxylic acid Template | MolDraw"
url: https://www.moldraw.com/templates/grignard-carboxylation/
description: "Grignard reagent + CO₂ → carboxylic acid template: Phenylmagnesium bromide attacks the carbon of CO₂ (dry ice) to give the magnesium carboxylate, which acid…"
lang: en
publisher: Scidart Academy
generated: 2026-11-13
---
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# Grignard reagent + CO₂ → carboxylic acid template

![Grignard reagent + CO₂ → carboxylic acid template: Phenylmagnesium bromide attacks the carbon of CO₂ (dry ice) to give the magnesium carboxylate, which acid work-up turns into benzoic acid.](https://www.moldraw.com/templates/grignard-carboxylation.webp)

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Phenylmagnesium bromide attacks the carbon of CO₂ (dry ice) to give the magnesium carboxylate, which acid work-up turns into benzoic acid.

## Mechanism step by step

Carboxylation with dry ice adds one carbon; acid work-up frees the acid

1. **Addition to CO₂** – The C–Mg bond attacks the CO₂ carbon; a C=O becomes C–O⁻
2. **Acid work-up** – Aqueous acid protonates the carboxylate

## Key points

- Adds one carbon: R–X → R–MgX → R–COOH. It works for aryl, vinyl and tertiary halides, where the nitrile route (SN2 with CN⁻) fails.
- The carboxylate salt is negatively charged and unreactive, so a second equivalent does not add (unlike an ester).
- The Grignard solution is poured onto excess crushed dry ice, protected from moist air; any water would give benzene instead.
- ¹³CO₂ or ¹⁴CO₂ puts an isotope label on the carboxyl carbon only.

Drawn with 63 atoms, 7 arrows, 8 shapes – every one editable in MolDraw.

## Sources

- [Clayden, Greeves & Warren, Organic Chemistry, 2nd ed., OUP 2012, ch. 9](https://openlibrary.org/isbn/9780199270293) Textbook
- [Kürti & Czakó, Strategic Applications of Named Reactions in Organic Synthesis, Elsevier 2005](https://openlibrary.org/isbn/9780124297852) Textbook

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## Frequently asked questions

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