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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63810Generated: October 26, 2026

7,9,10-Trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthrene → HCID 58771208, compound

https://huagongshe.com/reaction/63810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7,9,10-Trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthreneHCID 68497100—
CatalystSulfuric AcidHCID 1118—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 58771208HCID 58771208105.3%

Reaction Steps

A solution of 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) (180 mg of crude material form above) in AcOH (10 mL) and conc. H2SO4 (10 drops) was hydrogenated (H2, 50 psi, RT) with 5% Pd/C (20 mg of 50% w/w wet) at RT for 16 h. The reaction mixture was then filtered through celite. The celite was rinsed with DCM (2×2 mL). The DCM layer was concentrated by rotary evaporation to yield a light brown oil. The oil was dissolved in DCM (15 mL) and passed through a silica plug. The DCM was concentrated by rotary evaporation to yield (R,R,R)-5-butyl-2,7,8-trimethyl-2-(4,8,12-trimethyl-tridecyl)-chroman-6-ol (Ex-1C-3) as a cloudy yellow oil (165 mg, >100%), which was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447006B2
Source datasetuspto-grants-2016_09
ORD IDord-c0ef363922ba4be6bd1e4b73cee54562
Source noteuspto-grants-2016_09