HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747227Generated: November 1, 2026
Chloroacetyl chloride → HCID 118117511, compound
https://huagongshe.com/reaction/1747227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 89560151 | HCID 89560151 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118117511 | HCID 118117511 | — |
Reaction Steps
NaOH 1M aq. soln. (10 mL) followed by NaOH 32% (270 μL) were added to a 0° C. solution of rac-2-amino-3-(3-iodo-phenyl)-2-methyl-propan-1-ol H-6 (850 mg, 2.92 mmol) in DCM (10 mL). After 10 min a solution of chloroacetyl chloride (261 mL, 3.21 mmol) in DCM (10 mL) was added dropwise to the reaction mixture maintaining the temperature below 5° C. The resulting suspension was heated to 35° C. for 30 min after which complete formation of product was observed by LCMS. The layers were separated and the aqueous layer extracted with DCM (2×). The combined organic extracts were washed with brine, dried over Na2SO4, filtered and evaporated in vacuo to give the title compound that was used further without purification. LC-MS A: tR=0.79 min; [M(35Cl)+H]+=367.91.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150566B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-c051643baa96440b886884fa221d9a87 |
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| Source note | uspto-grants-2015_10 |
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