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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542138Generated: October 25, 2026

Diisopropylamine → HCID 178469143, compound

https://huagongshe.com/reaction/542138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantAcetic acid, 2-chloro-2,2-difluoro-, ethyl esterHCID 67843—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178472209HCID 178472209—
SolventDiethyl EtherHCID 3283—
ProductHCID 178469143HCID 17846914378%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To 85 ml of dry ether and 21.4 ml (0.152 mol) of diisopropylamine at -78° C. was added 97 ml (0.150 mol) of 1.55M n-BuLi. After stirring at -78° C. for 20 minutes a solution of 16.3 g (0.068 mol) of product of Example 34 in 10 ml of dry ether was added. After stirring at -78° C. for 1 hour, 35 g (0.221 mol) of ethyl chlorodifluoroacetate was added. Stirring at -78° C. was continued for 1 hour and then warmed to room temperature in 11/2 hour. The reaction mixture was poured into 200 ml of ice water and extracted with ether. The ether was extracted with 15% K2CO3 and water. The water extracts were combined, acidified with concentrated HCl and extracted with ether. The original aqueous layer was acidified with concentrated HCl, extracted with ether and combined with the above ether extract, dried (MgSO4) and concentrated in vacuo affording 17.7 g of solid. This solid was heated on the kugelrohr apparatus at 125° C. for 1/2 hour at atm. pressure and then distilled at 19 Pa, pot temperature 69° C. to give 13.57 g (59.8%) of product as a white solid; mp 37°-39° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04655816
Source datasetuspto-grants-1987_04
ORD IDord-884d5052cf714f31b3264affaf58a8df
Source noteuspto-grants-1987_04