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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852979Generated: October 29, 2026

Sulfuric Acid → HCID 58930409, compound

https://huagongshe.com/reaction/852979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDichloromethaneHCID 6344—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium HydroxideHCID 14798—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantHCID 57434763HCID 57434763—
ReactantHCID 57434764HCID 57434764—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 58930409HCID 5893040966%

Reaction Steps

3-[4-(1-Methyl-piperidin-4-yl)-butoxy]-benzaldehyde. To a stirred solution of 3-[4-(1-methyl-piperidin-4-yl)-butoxy]-benzonitrile (0.84 g, 3.09 mmol) in toluene (5 mL) at 0° C. was added 1.5 M DIBAL-H in toluene (4.63 mL, 4.63 mmol). After 3 h, methanol (9 mL) and 1.0 M H2SO4 (10 mL) were added dropwise. After stirring for 30 min, the solution was neutralized with 1.0 M sodium hydroxide (10 mL) followed by addition of satd. aq. sodium potassium tartrate (40 mL) and CH2Cl2 (100 mL). After stirring for 30 min the solution was extracted with CHCl3 (3×50 mL), washed with brine and dried over Na2SO4. Purification by Method 1 afforded 0.56 g (66%) of the title compound. 1H NMR (400 MHz, CDCl3): 9.97 (s, 1H), 7.46-7.43 (m, 2H), 7.39-7.37 (m, 1H), 7.19-7.15 (m, 1H), 4.02 (t, J=6.6, 2H), 2.86-2.80 (m, 2H), 2.25 (s, 3H), 1.92-1.83 (m, 2H), 1.83-1.75 (m, 2H), 1.73-1.63 (m, 2H), 1.54-1.44 (m, 2H), 1.34-1.18 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253200B2
Source datasetuspto-grants-2007_08
ORD IDord-8c138ce81e9646209d8569d4fbbe2fa7
Source noteuspto-grants-2007_08