HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 3-Methoxycarbonyladamantane-1-carboxylic Acid Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-(Methoxycarbonyl)adamantane-1-carboxylic acid | HCID 365222 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxycarbonyladamantane-1-carboxylic Acid Chloride | HCID 54178337 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
3-Methoxycarbonyladamantane-1-carboxylic acid (1.0 eq) was suspended in a solution of CH2Cl2 containing a catalytic amount of DMF. This mixture was then cooled to 0° C. and oxalyl chloride (3.0 eq) was added. After 15 minutes, the reaction mixture was allowed to warm to room temperature and stirred at this temperature for 30 minutes, and then warmed to reflux for 1 hour. During the reflux period, the reaction became homogenous. The reaction mixture was then cooled and concentrated at reduced pressure. The residue was taken-up in diethyl ether and filtered. The filtrate was concentrated at reduced pressure to yield the title intermediate as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06465513B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-e377fe0466ae4a30a84e0807c55b7ac7 |
| Source note | uspto-grants-2002_10 |