Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501793Generated: October 29, 2026

Formaldehyde → HCID 23021572, compound

https://huagongshe.com/reaction/501793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantHCID 22497995HCID 22497995—
SolventTolueneHCID 1140—
SolventTributylamineHCID 7622—
SolventTin tetrachlorideHCID 24287—
ProductHCID 23021572HCID 2302157222.6%

Reaction Steps

2.90 g of 3-cyclopentylphenol was dissolved in 14.5 mL of toluene, to which 0.21 mL of tin tetrachloride and 1.7 mL of tri-n-butylamine were added at room temperature in a stream of nitrogen, and then this mixture was stirred for 30 minutes at room temperature followed by addition thereto of 1.18 g of paraformaldehyde, and this mixture was stirred for 1.5 hours at 80° C. Then, the reaction mixture was cooled to room temperature and poured into water, to which methylene chloride was added, and then the organic phase was separated therefrom. After the resultant organic phase was washed with water and a saturated sodium chloride solution successively, the washed phase was dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure. The resultant residue was purified by silica gel column chromatography [eluent; hexane:ethyl acetate=10:1] to yield 0.77 g of 4-cyclopentyl-2-hydroxybenzaldehyde as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772285B2
Source datasetuspto-grants-2010_08
ORD IDord-1147e87d9f184ae6bcf70f202cbe577c
Source noteuspto-grants-2010_08