Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725326Generated: November 1, 2026

HCID 74020198, compound → HCID 74020197, compound

https://huagongshe.com/reaction/1725326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 74020198HCID 74020198—
ReactantHCID 178418348HCID 178418348—
ProductHCID 74020197HCID 74020197—

Reaction Steps

To a dry 5 liter multi-neck round bottom flask fitted with an air stirrer, nitrogen inlet condenser and an addition funnel 1.617 g of CH3Li was added and stirred. 336 g of 4-methyl-3-decene-5-one (see example A for preparation of 3-decene-4-methyl-5-one) was added dropwise over 105 minutes. The temperature of the reaction rose to 63° C. The reaction mixture was aged for 150 minutes and a first sample was taken at 37° C. 30 minutes later, a second sample was taken at 30° C. The mixture was quenched with acetic acid, allowed to settle and layers separated. The aqueous layer was washed twice with 100 ml of toluene. The toluene extracts were added to the organic layer and washed with Na2CO3. The NMR spectrum of the 4.5-Dimethyl-3-decene-5-ol is as follows: 0.88 ppm (t, 3H); 0.94 ppm (t, 3H); 1.28 ppm (s, 3H); 1.15-1.35 ppm (m, 6H); 1.50 ppm (s, 1H); 1.55 ppm (s,1H), 2.05 ppm (m, 2H); ; 5.45 ppm (m, 1 H) The IR spectrum of the 4.5-Dimethyl-3-decene-5-ol is as follows: OH-stretch broad at 3416 cm−1, CH-stretch saturated at 2960, 2933, 2872 cm−1, double bond stretch at 1680 cm−1, 1462 and 1372 due to CH stretch.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491684B2
Source datasetuspto-grants-2009_02
ORD IDord-0ceae287d09341dfaa60e642f7839971
Source noteuspto-grants-2009_02