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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061291Generated: November 1, 2026

Dichloromethane → [4-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-phenyl]-methanol

https://huagongshe.com/reaction/1061291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-(1,4-Dioxa-8-azaspiro[4.5]decan-8-yl)benzaldehydeHCID 2764335—
ReactantSodium borohydrideHCID 4311764—
SolventMeOH tetrahydrofuranHCID 21899815—
Product[4-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-phenyl]-methanolHCID 10586716—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (3.78 g, 100 mmol) was added in four portions to a stirred solution of 4-(1,4-dioxa-8-aza-spiro[4.5]dec-8-yl)-benzaldehyde (4.94 g, 20 mmol) (Taylor, E. C., Skotnicki, J. S. Synthesis, 1981, 606) in methanol/tetrahydrofuran (1:1, 100 mL) at 0° C. and the resulting solution was stirred at 0° C. for 30 minutes and then at room temperature for 1 hour. Methylene chloride was added and the solution was washed with water and dried over sodium sulfate. The solvents were removed and the residue was solidified upon standing (5.0 g, 100%); 1H NMR (300 MHz, CDCl3) δ 1.84 (t, J=5.7 Hz, 4H), 3.33 (t, J=5.7 Hz, 4H), 3.99 (s, 4H), 4.59 (d, J=5.8 Hz, 2H), 6.93 (d, J=8.7 Hz, 2H), 7.24 (d, J=8.7 Hz, 2H); MS (ES) m/z: 249.9 (MH+); HRMS Calcd. for C14H20NO3 (MH+): 250.1443. Found: 250.1434.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-a38d6f40f05f4723b72e72937d576f4b
Source noteuspto-grants-2003_02