Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (6S)-6-(Propylamino)-5,6,7,8-tetrahydronaphthalen-1-ol | HCID 10219902 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86748409 | HCID 86748409 | 81.3% |
Reaction Steps
A stirring suspension of (S)-6-propylamino-5,6,7,8-tetrahydro-l-naphthalenol (7.34 g, 0.0257 mol) in water (100 mL) was cooled in an ice bath and sodium bicarbonate (8.49 g, 0,101 mol) was added. This suspension was stirred for fifteen minutes then benzyl chloroformate (4.50 g, 0.0264 mol) was added dropwise. The mixture was stirred for fifteen minutes and then allowed to come to room temperature. Ether (100 mL) was added and the mixture was stirred overnight. The layers were separated and the aqueous layer was extracted with ether. The combined organic layers were washed twice with saturated aqueous sodium bicarbonate, once with water, twice with dilute hydrochloric acid, once with water and once with saturated aqueous sodium chloride, dried (magnesium sulfate) and concentrated under reduced pressure to give 7.09 g (81% yield) of product as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05382596 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-55cfc5a86d324534b531e1ad06d969f2 |
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| Source note | uspto-grants-1995_01 |
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