HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 2-[4-(Tert-butyldimethylsilyloxy)phenyl]acetyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-{4-[(Tert-butyldimethylsilyl)oxy]phenyl}acetic acid | HCID 610618 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[4-(Tert-butyldimethylsilyloxy)phenyl]acetyl chloride | HCID 12188707 | — |
Reaction Steps
Under an argon atmosphere, to a mixture of 2-[4-(tert-butyldimethylsilyloxy)phenyl]acetic acid (9) (1.55 g, 5.82 mmol) in CH2Cl2 (10 mL) was added DMF (3 drops) by a Pasteur pipette at room temperature. To this was added oxalyl dichloride (985 μL, 11.6 mmol) at 0° C. and the mixture was stirred for 30 minutes while elevating to room temperature. The mixture was concentrated under reduced pressure to give crude 2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride (10) as a colorless oil, which was used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642281B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-1ebbf246347d4152adb36fcbc00edfd8 |
| Source note | uspto-grants-2014_02 |