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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198768Generated: October 30, 2026

Acetic Anhydride → HCID 12899886, compound

https://huagongshe.com/reaction/2198768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3,3-Bisfluoromethyl-1-(4-chlorophenoxy)-1-(1,2,4-triazol-1-yl)-butan-2-olHCID 12899883—
ProductHCID 12899886HCID 12899886—

Reaction Conditions

Temperature100 °C

Reaction Steps

112 g (0.328 mol) of 3,3-bisfluoromethyl-1-(4-chlorophenoxy)-1-(1,2,4-triazol-1-yl)-butan-2-ol (as the diastereomeric mixture of the pure forms A and B) were dissolved in 500 ml of acetic anhydride. The solution was stirred at 100° C. for 16 hours, the excess acetic anhydride was distilled off in vacuo and the residue was taken up in 600 ml of methylene chloride. The organic phase was washed twice with 1.5 liters of water each time, dried over sodium sulphate and concentrated. The oily residue was subjected to fractional crystallization in diisopropyl ether. 48 g (38% of theory) of the A-form (Compound 1a) of 2-acetoxy-3,3-bisfluoromethyl-1-(4-chlorophenoxy)-1-(1,2,4-triazol-1-yl)-butane of melting point 130°-133° C. and 20.5 g (16% of theory) of the B-form (Compound 1b) of 2-acetoxy-3,3-bisfluoromethyl-1-(4-chlorophenoxy)-1-(1,2,4-triazol-1-yl)-butane of melting point 98° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04359470
Source datasetuspto-grants-1982_11
ORD IDord-927c1fe99516406b85d0b802728066c9
Source noteuspto-grants-1982_11