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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050158Generated: November 2, 2026

Phenol → 1-Chloro-3-phenoxy-2-propanol

https://huagongshe.com/reaction/2050158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantEpichlorohydrinHCID 7835—
ReactantPiperidine, hydrochloride (1:1)HCID 2723721—
Product1-Chloro-3-phenoxy-2-propanolHCID 94300—

Reaction Steps

A mixture of phenol (94g; 1.0 mole) and epichlorhydrin (138.8g; 1.5 mole) was vigorously stirred at 100° C. in the presence of piperidine hydrochloride (2.0g) for 6 hours, cooled, and the excess epichlorhydrin removed at 100° in vacuo. The residue was cooled, dissolved in an equal volume of chloroform and stirred vigorously with excess concentrated hydrochloric acid for 0.5 hours. After separation of the phases the organic layer was washed with water, dried and evaporated to a colourless oil. Distillation gave 116.4g (62.5%) of 1-chloro-3-phenoxy-2-propanol of bp0.6 112° as a GLC pure material, νmax (film) 3310, 1603, 1590, 1495, 1245cm-1 ; τ(CSCl3); 7.40 (broad exchangeable s); 6.25 (2H, d, J 3.5 Hz); 5.90 (2H, s); 5.90 (1H, m); 3.21-2.56 (5H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200577
Source datasetuspto-grants-1980_04
ORD IDord-303f573a7d3e46b68c2588bc267d44c3
Source noteuspto-grants-1980_04