HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085978Generated: November 1, 2026
Ethyl chloroformate → HCID 22726773, compound
https://huagongshe.com/reaction/2085978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 3-TERT-BUTYLTHIO-2-CARBOXYPYRIDINE | HCID 11830727 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22726773 | HCID 22726773 | — |
Reaction Steps
To a suspension of 3-t-butylthio-2-carboxypyridine (10.0 g, 47.4 mmol) in tetrahydrofuran (200 mL) cooled to −5° C. was added trethylamine (8.25 mL, 47.4 mmol) followed by addition of ethyl chloroformate (4.38 g, 47.4 mmol) and reaction was stirred for 30 min at 0° C. Lithium borohydride (2.58 g, 118 mmol) was added in portions, maintaining the temperature below 5° C. After the addition was complete the reaction was allowed to warm to room temperature and stirred for 1 hour. Temperature was lowered to −5° C. and methanol (10 mL) was added followed by addition of aqueous sodium hydroxide (10 mL, 10%). After addition of ethyl acetate (50 mL) and water (40 mL) dilute hydrochloric acid was added to pH=5.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06723716B1 |
|---|
| Source dataset | uspto-grants-2004_04 |
|---|
| ORD ID | ord-fa4526f156c44bcfa1e91beefc544788 |
|---|
| Source note | uspto-grants-2004_04 |
|---|