Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013002Generated: October 30, 2026

Chloroacetaldehyde → HCID 178523005, compound

https://huagongshe.com/reaction/1013002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178511399HCID 178511399—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 178523005HCID 178523005—

Reaction Steps

To a stirred suspension of compound of Step 3 in dry trimethylortoformiate, triethylamine (1.3 eq.) and 1.1 eq. of α-chloroacetaldehyde (1.1 eq.) were added. The resulting solution was aged for 2 hours at room temperature, the solvent was removed by rotary evaporation to afford a residue that was dissolved in MeOH, treated with acetic acid (pH=5) and NaBH3CN (1.1 eq.). The mixture was stirred overnight at room temperature then the solvent was removed by rotary evaporation and the resulting residue was taken in dry toluene and concentrated. This material was used without any purification for the next step. MS (ES) C23H24ClFN4O4 requires 474. Found: 475.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981879B2
Source datasetuspto-grants-2011_07
ORD IDord-457ef0f7d4d841bfb66de8aa126b8750
Source noteuspto-grants-2011_07