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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033943Generated: October 25, 2026

Water → 1-Phenoxy-2-propanol

https://huagongshe.com/reaction/1033943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
Reactant1-Phenoxy-2-propanoneHCID 69313—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product1-Phenoxy-2-propanolHCID 9283985%

Reaction Conditions

Temperature0 °C

Reaction Steps

Phenoxy-2-propanone (3.4 mL, 25 mmol) was dissolved in ethanol (30 mL) and cooled to 0° C. Sodium borohydride (0.95 g; 25 mmol; 1 equiv.) was added. The mixture was stirred and allowed to warm to room temperature overnight. All of the starting material was gone according to tlc analysis, so the mixture was poured into water (30 mL) and ether (30 mL). The layers were separated and the aqueous layer was extracted with ether (2×20 mL). The organic layers were combined and concentrated. The resulting aqueous residue was poured into ether (25 mL). The organic layer was removed, dried (MgSO4), and concentrated to provide 1e (3.2 g; 85%). 1H nmr (300 MHz, CDCl3): 7.332-7.261 (3H, m); 6.995-6.904 (2H, m); 4.15-4.24 (1H, m); 3.972-3.768 (2H, m); 1.559 (1H, s); 1.290 (3H, d, J=6.38 Hz). IR (neat film, cm-1): 3350 (b, s); 2900 (s); 1590 (m). EIMS (m/e): 152 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312950
Source datasetuspto-grants-1994_05
ORD IDord-a92c87fe015d4d3ba7d770b991676f8e
Source noteuspto-grants-1994_05