Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63809Generated: October 25, 2026

Acetic Acid → 7,9,10-Trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthrene

https://huagongshe.com/reaction/63809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantButanalHCID 261—
ReactantEthyl AcetateHCID 8857—
Reactant(+)-gamma-TocopherolHCID 92729—
CatalystSulfuric AcidHCID 1118—
SolventWaterHCID 962—
Product7,9,10-Trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthreneHCID 68497100100%

Reaction Steps

A 25 mL RBF was charged with butyraldehyde (155 mg, 2.16 mmol), AcOH (2 mL) and H2SO4 (1 drop). To the flask was then added a solution of (+)-γ-tocopherol (Ex-1C-1) (300 mg, 0.72 mmol) in AcOH (3 mL) dropwise over 2 h via syringe pump. The reaction was then stirred for 16 h and monitored by TLC (9:1 Hept:EtOAc). The reaction was then diluted with water (15 mL) and extracted with DCM (3×20 mL). The combined organic layers were washed with water (3×15 mL), dried over Na2SO4, filtered and concentrated by rotary evaporation to yield 7,9,10-trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthrene (Ex-1C-2) as a brownish oil (425 mg, >100%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447006B2
Source datasetuspto-grants-2016_09
ORD IDord-128bc00887994050a25505632883fba9
Source noteuspto-grants-2016_09