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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274712Generated: November 2, 2026

3-Chloro-1,1-diethoxypropane → HCID 71294568, compound

https://huagongshe.com/reaction/2274712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-1,1-diethoxypropaneHCID 96217—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86678087HCID 86678087—
SolventTolueneHCID 1140—
ProductHCID 71294568HCID 71294568457.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of the diol (6Z,9Z,29Z,32Z)-octatriaconta-6,9,29,32-tetraene-18,20-diol (7) (940 mg, 1.68 mmol) and 3-chloropropionaldehyde diethylacetal (563 μL, 3.36 mmol) in toluene (15 mL) was treated with PPTS (50 mg) and heated (80° C., 2 h). After cooling (rt) the reaction mixture was poured into sat. aq. NaHCO3, extracted with EtOAc, washed with brine, dried (Na2SO4), filtered and concentrated. The crude product was dissolved in a solution of (CH3)2NH (25 mL, 5.6M in EtOH), transferred to a sealed reaction vessel and heated (80° C., 16 h). Once complete the yellow solution was concentrated and the residue was subjected to chromatography (100% EtOAc) to yield 2-(4-((8Z,11Z)-heptadeca-8,11-dien-1-yl)-6-((9Z,12Z)-octadeca-9,12-dien-1-yl)-1,3-dioxan-2-yl)-N,N-dimethylethanamine (8) (585 mg, 54% over 2 steps) as a pale yellow oil. Rf 0.5 (10% CH3OH—CH2Cl2); 1H NMR (400 MHz, CDCl3) 5.46-5.29 (m, 8H), 4.85 (t, 0.5H), 4.59 (t, 0.5H), 4.08-3.98 (m, 0.5H), 3.80-3.70 (m, 0.5H), 3.60-3.50 (m, 1H), 2.78 (app. t, 4H), 2.50-2.37 (m, 2H), 2.32-2.21 (m, 6H), 2.13-2.02 (m, 8H), 1.88-1.72 (m, 2H), 1.63-1.22 (m, 40H), 0.91 (t, 6H). FW 643.47, C43H79NO2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126966B2
Source datasetuspto-grants-2015_09
ORD IDord-fd4a340b06494d71a7926d39facf1d22
Source noteuspto-grants-2015_09