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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229221Generated: November 2, 2026

1,2-Dichloroethane → HCID 86758351, compound

https://huagongshe.com/reaction/2229221

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAcetic AcidHCID 176—
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
ReactantHCID 15511753HCID 15511753—
SolventWaterHCID 962—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 86758351HCID 86758351—

Reaction Conditions

Temperature75 °C

Reaction Steps

A biphasic suspension of 2.43 g (7.35 mmol) of the compound obtained in Step D of Example 1 and 1.33 ml (10.29 mmol) of 2,5-dimethoxytetrahydrofuran in a mixture of 24 ml of distilled water, 12 ml of acetic acid and 36 ml of 1,2-dichloroethane is stirred vigorously at 75° C. for 60 minutes. In TLC (CH2Cl2/MeOH 9:1), a small amount of starting material is still observed. 0.2 eq. of 2,5-dimethoxytetrahydrofuran (2.06 mmol, 0.26 ml) is added, and heating is maintained for 30 minutes. The mixture is left to return to room temperature and extraction is carried out with CH2Cl2. The organic phase is washed 4 times with water and then with a saturated NaCl solution. Drying is carried out over MgSO4, followed by evaporation and chromatography of the resulting oil over 200 g of Merck 7734 silica whilst eluting with a mixture of CH2Cl2/MeOH 95:5. An oil corresponding to the title product is obtained, which is crystallised from isopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420386B1
Source datasetuspto-grants-2002_07
ORD IDord-110df0efd9fd49ad8c8f6841ba6f8c03
Source noteuspto-grants-2002_07