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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706454Generated: November 2, 2026

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

https://huagongshe.com/reaction/1706454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantEpichlorohydrinHCID 7835—
CatalystPiperidine, hydrochloride (1:1)HCID 2723721—
Product1-Chloro-3-phenoxy-2-propanolHCID 9430062.5%

Reaction Steps

A mixture of phenol (94 g; 1.0 mole) and epichlorhydrin (138.8 g; 1.5 mole) was vigorously stirred at 100° C. in the presence of piperidine hydrochloride (2.0 g) 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 116.4 g (62.5%) of 1-chloro-3-phenoxy-2-propanol of bp0.6 112° as a GLC pure material, νmax (film) 3310, 1603, 1590, 1495, 1245 cm-1 ; τ(CDCl3); 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 numberUS04207335
Source datasetuspto-grants-1980_06
ORD IDord-9ffca8f774504449bb8aee984e2b00d3
Source noteuspto-grants-1980_06