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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916365Generated: October 31, 2026

Water → 4-(2-Methoxy-4-nitrophenyl)but-3-en-2-ol

https://huagongshe.com/reaction/1916365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantCID 67066682HCID 67066682—
SolventEthanolHCID 702—
Product4-(2-Methoxy-4-nitrophenyl)but-3-en-2-olHCID 67066678100%

Reaction Steps

To a suspension of 4-(2-methoxy-4-nitrophenyl)but-3-en-2-one (12.2 g; 55.2 mmol) in 150 mL of ethanol at rt was added NaBH4 (2.30 g; 60.7 mmol) over 5 minutes. The suspension was stirred at rt for 1 h, diluted with 1M NaHPO4 (˜60 mL) followed by water (100 mL) and concentrated under reduced pressure to remove ethanol. After extracting the aqueous residue with CH2Cl2, the organic layer was washed with water and brine, dried over anhydrous MgSO4, filtered. Concentration of the filtrate under reduced pressure afforded 12.3 g (100%) of the title compound as a dark, red gum. HPLC (Method #1) 3.68 min retention time, (50%); MS (ES): m/z 206 [M−OH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618115B2
Source datasetuspto-grants-2013_12
ORD IDord-95b891da4ff24113b652ae356b2a3bd9
Source noteuspto-grants-2013_12