HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747210Generated: October 31, 2026
Chloroacetyl chloride → HCID 118117773, compound
https://huagongshe.com/reaction/1747210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 118117637 | HCID 118117637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118117773 | HCID 118117773 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09150566B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-8fa3064a717d4ce4baec3e6895e4e4f7 |
|---|
| Source note | uspto-grants-2015_10 |
|---|