HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-3-iodopropane → Methyl 2-hydroxy-2-(4-methoxyphenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-3-iodopropane | HCID 81363 | — |
| Reactant | Methyl methoxy-(4-methoxyphenyl)acetate | HCID 10262525 | — |
| Reactant | Methyl 5-chloro-2-methoxy-2-(4-methoxyphenyl)valerate | HCID 67067429 | — |
| Product | Methyl 2-hydroxy-2-(4-methoxyphenyl)acetate | HCID 523496 | — |
Reaction Steps
246 mg of a mixture of methyl 5-chloro-2-methoxy-2-(4-methoxyphenyl)valerate with methyl methoxy-(4-methoxyphenyl)acetate was obtained from methyl hydroxy-(4-methoxyphenyl)acetate (724 mg) and 1-chloro-3-iodopropane (0.56 ml) by the same method as in Examples 85 and 86. Then, the ester mixture was hydrolyzed and amidated with tert-butyl carbazate according to the method in Examples 85 and 86 to obtain 32 mg of tert-butyl N′-[5-chloro-2-methoxy-2-(4-methoxyphenyl)pentanoyl]hydrazinecarboxylate and 122 mg of tert-butyl N′-[2-methoxy-2-(4-methoxyphenyl)acetyl]hydrazinecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713993B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-1ddb5f626ee14ed798ea1730311faad3 |
| Source note | uspto-grants-2010_05 |