HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → alpha-(1-Ethoxymethyl-5-pyrazolyl)-2,3-dichloro-4-ethoxycarbonylmethoxybenzylalcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | alpha-(1-Ethoxymethyl-5-pyrazolyl)-2,3-dichloro-4-hydroxybenzylalcohol | HCID 14622794 | — |
| Product | alpha-(1-Ethoxymethyl-5-pyrazolyl)-2,3-dichloro-4-ethoxycarbonylmethoxybenzylalcohol | HCID 20030167 | 98% |
Reaction Steps
634 mg of α-(1-ethoxymethyl-5-pyrazolyl)-2,3-dichloro-4-hydroxybenzylalcohol and 367 mg of ethyl bromoacetate are treated in the same manner as described in Example 1 to give 790 mg of α-(1-ethoxymethyl-5-pyrazolyl)-2,3-dichloro-4-ethoxycarbonylmethoxybenzylalcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04853404 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-d72d35cb89a64b19b546944f583191ce |
| Source note | uspto-grants-1989_08 |