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Williamson Ether Synthesis: Mechanism & Rules

By Chemca Editorial Team • Last Updated: January 2026 • 10 min read

The Williamson Ether Synthesis is the most important laboratory method for the preparation of symmetrical and unsymmetrical ethers. It involves the reaction of an Alkyl Halide with a Sodium Alkoxide.

1. General Reaction

A sodium or potassium alkoxide reacts with a primary alkyl halide to form an ether and a metal halide salt.

$$ R-X + R'-O^-Na^+ \xrightarrow{\Delta} R-O-R' + NaX $$

Key Components:

• Substrate ($R-X$): Must be Methyl or Primary ($1^\circ$) Alkyl Halide.
• Reagent ($R'O^-$): Sodium/Potassium Alkoxide (can be $1^\circ, 2^\circ, 3^\circ$ or Phenoxide).
• Mechanism: $S_N2$ (Nucleophilic Substitution Bimolecular).

2. Detailed Mechanism

The reaction follows a concerted $S_N2$ mechanism involving the backside attack of the alkoxide ion on the alkyl halide.

Single Step Process

The alkoxide ion acts as a strong nucleophile and attacks the carbon bonded to the halogen from the side opposite to the leaving group.

$$ R'-O:^- + R-X \rightarrow [R'-O \dots R \dots X]^- \rightarrow R'-O-R + X^- $$

Since it is an $S_N2$ reaction, inversion of configuration occurs if the chiral center is attacked.

3. The Limitation: Elimination vs. Substitution

This is the most critical concept for exams. Alkoxides are not only good nucleophiles but also strong bases.

The Rule of Steric Hindrance

• Best Case: Primary Alkyl Halide ($1^\circ$). Reaction proceeds via $S_N2$ to form Ether.
• Failure Case: Tertiary Alkyl Halide ($3^\circ$). Steric hindrance prevents nucleophilic attack. The alkoxide acts as a base, causing Elimination ($E2$) to form an Alkene.
• Secondary Alkyl Halide ($2^\circ$): Gives a mixture of Ether and Alkene.

4. Strategic Examples

Preparation of t-Butyl Methyl Ether (MTBE)

To prepare an ether with a bulky group, the bulky group must come from the Alkoxide, not the Halide.

Correct Method:

$$ CH_3-Br + (CH_3)_3C-O^-Na^+ \rightarrow (CH_3)_3C-O-CH_3 + NaBr $$

Result: Ether Formation (Substrate is Methyl bromide - unhindered).

Incorrect Method:

$$ (CH_3)_3C-Br + CH_3-O^-Na^+ \rightarrow CH_2=C(CH_3)_2 + CH_3OH + NaBr $$

Result: Elimination to Isobutylene (Substrate is $3^\circ$ halide).

5. Reaction with Phenols

Phenols are converted to Phenoxides using NaOH, which then react with primary alkyl halides to form Aryl Alkyl Ethers (like Anisole).

$$ C_6H_5OH \xrightarrow{NaOH} C_6H_5O^-Na^+ \xrightarrow{CH_3I} \underbrace{C_6H_5-O-CH_3}_{\text{Anisole}} + NaI $$

Note: Aryl halides ($Ar-X$) cannot be used as the substrate because they do not undergo nucleophilic substitution easily.

6. Intramolecular Williamson Synthesis

If a molecule contains both a halogroup and a hydroxyl group (halohydrin), treating it with base leads to Intramolecular $S_N2$, forming cyclic ethers (Epoxides).

Williamson Quiz

Test your concepts on Ether Synthesis. 10 MCQs with explanations.

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