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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747210Generated: October 31, 2026

Chloroacetyl chloride → HCID 118117773, compound

https://huagongshe.com/reaction/1747210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
ReactantHCID 118117637HCID 118117637—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118117773HCID 118117773—

Reaction Conditions

Temperature0 °C

Reaction Steps

Chloroacetylchloride (1.05 mL, 13.1 mmol) was added dropwise to a 0° C. solution of (R)-2-amino-3-(3-iodo-phenyl)-propan-1-ol A-8 (3.03 g, 10.9 mmol) and Et3N (1.98 mL, 14.2 mmol) in THF (50 mL) under argon and the resulting suspension was warmed to RT and stirred for 30 min. The reaction mixture was cooled back to 0° C. before being quenched with water and concentrated in vacuo. The remaining aq. phase was extracted with EtOAc (2×) and the combined organic extracts were washed with brine, dried over Na2SO4, filtered and evaporated in vacuo to give the title compound as a cream solid that was used further without purification. LC-MS B: tR=0.71 min; [M(35Cl)+H]+=353.75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150566B2
Source datasetuspto-grants-2015_10
ORD IDord-8fa3064a717d4ce4baec3e6895e4e4f7
Source noteuspto-grants-2015_10