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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633444Generated: November 1, 2026

Ethyl Acetate → 2-(4-Amino-2-chlorophenoxy)ethan-1-ol

https://huagongshe.com/reaction/633444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantStannous chloride dihydrateHCID 61436—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl-(2-(2-chloro-4-nitrophenoxy)ethoxy)dimethylsilaneHCID 86704535—
SolventEthanolHCID 702—
Product2-(4-Amino-2-chlorophenoxy)ethan-1-olHCID 196227613.4%

Reaction Steps

A mixture of tert-butyl-(2-(2-chloro-4-nitrophenoxy)ethoxy)dimethylsilane (475 mg, 1.4 mmol) and SnCl2.2H2O (1.07 g, 5.7 mmol) in EtOH (40 mL) was heated to reflux and stirred for 4 hr. After allowing to cool, the mixture was poured into EtOAc (50 mL) and saturated NaHCO3 (50 mL), then filtered through celite. The filtrate was partitioned and the aqueous layer extracted with EtOAc (2×50 mL). The combined organic layers were dried (Na2SO4), filtered and concentrated under vacuum to leave a crude residue. The residue was dry-loaded on to silica gel and purified by column chromatography on silica gel using EtOAc/heptane (2:8 to 1:0) as eluent to give the product (9 mg, 3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321763B2
Source datasetuspto-grants-2016_04
ORD IDord-59aa6dec782d493294b5142e45056e38
Source noteuspto-grants-2016_04