Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 10888839 | HCID 10888839 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69916876 | HCID 69916876 | 77% |
Reaction Steps
Triethylamine (11.8 mL, 84.6 mmol) was added to a solution of 4-(dimethoxymethyl)benzoic acid (11.0 g, 56.4 mmol, prepared as described in Tetrahedron 1998, 54,15679-15690) in dichloromethane (120 mL) at room temperature. The reaction mixture was cooled to −40° C., ethyl chloroformate (6.7 mL, 70.0 mmol) was added dropwise, and stirring continued at −40° C. for 30 min. Hydrazine (8.85 mL, 282 mmol) was added and the reaction mixture was warmed to room temperature and stirred for an additional 1 h. The reaction mixture was diluted with dichloromethane, washed with water, dried with Na2SO4, and concentrated in vacuo to give 9.06 g (77%) of the title compound, which was used in the next step without further purification. MS 211 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825170B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-f8b8b29ab23245bc9823ec73bcde2c2e |
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| Source note | uspto-grants-2004_11 |
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