HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → alpha-Acetylamino-10,11-dihydro-5H dibenzo[a,d]cycloheptene-5-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Amino-2-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)acetic acid hydrochloride | HCID 67805603 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | alpha-Acetylamino-10,11-dihydro-5H dibenzo[a,d]cycloheptene-5-acetic acid | HCID 19385928 | 47.2% |
Reaction Steps
α-Amino-10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-acetic acid, hydrochloride (5.0 g, 16.5 mmol) is dissolved in 1N sodium hydroxide (70 mL) and 50 mL of water, cooled in an ice bath, and treated with acetic anhydride (2.3 mL, 25 mmol) keeping pH at 10 to 10.5. The mixture is stirred for an additional 20 minutes, then the pH is adjusted to 3 to 4 with concentrated hydrochloric acid. A precipitate is collected, washed with water, diethyl ether, and dried in a vacuum oven (50° C./10 mm Hg). The dried solid is recrystallized from ethyl acetate-hexane to give 2.41 g of the title compound; mp 220°-223° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380925 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-5c95aa978ae8438d89688b55c61bf3c2 |
| Source note | uspto-grants-1995_01 |