HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166045Generated: October 30, 2026
Ethyl bromoacetate → HCID 178519465, compound
https://huagongshe.com/reaction/2166045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-hydroxy-alpha-phenyl-1H-benzotriazole-6-methanol | HCID 14990621 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178519465 | HCID 178519465 | 68.8% |
Reaction Steps
To a stirred solution of 5.2 parts of 1-hydroxy-α-phenyl-1H-benzotriazole-6-methanol in 30 parts of dimethyl sulfoxide were added 0.96 parts of a sodium hydride dispersion 50%. The reaction mixture was stirred till no more hydrogen escapted. After the addition of 3.34 parts of ethyl 2-bromoacetate, the whole was stirred for 30 minutes at room temperature. 1.38 Parts of potassium carbonate were added and stirring was continued for 3 hours at 50° C. The dimethyl sulfoxide layer was evaporated and the residue was taken up in water and 20 parts of a hydrochloric acid solution 1N. The product was extracted with a mixture of trichloromethane and methanol (90:10 by volume). The extract was dried, filtered and concentrated. The concentrate was crystallized from 32.5 parts of dichloromethane. The product was filtered off and dried, yielding 3.1 parts (68.8%) of α-phenyl-1H-benzotriazole-5-methanol; mp. 143.0° C. (int. 70).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04943574 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-63f9a25f74f148f2b198e5698c6f4d83 |
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| Source note | uspto-grants-1990_07 |
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