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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163710Generated: November 1, 2026

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

https://huagongshe.com/reaction/2163710

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 separatiin 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(CDCl3); 7.40 (broad exchangeable s); 6.25 (2H, d, J 3.5Hz); 5.90 (2H, s); 5.90 (1H, m); 3.21-2.56 (5H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04136192
Source datasetuspto-grants-1979_01
ORD IDord-e90ef48ff3ae4383be47217d9334f113
Source noteuspto-grants-1979_01