Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 12595566 | HCID 12595566 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12595584 | HCID 12595584 | — |
Reaction Steps
8-isocyanato-8-(thiophen-2-yl)-1,4-dioxaspiro[4.5]decane (4 g) was dissolved in dry THF (140 ml) and the solution was cooled to 0°-10° C. LAH (4 g) was added in portions over a period of 30 minutes and the reaction mixture was heated for a further 30 minutes at 60° C. The mixture was cooled to 0°-10° C. and saturated ammonium chloride solution (100 ml) was added. The mixture was now filtered through celite and washed with ethyl acetate (3×150 ml). After removing the solvents the crude product was taken up in ethyl acetate (200 ml) and stirred for 3 minutes at 0°-10° C. The ethyl acetate phase was separated, and aqueous phase was made alkaline (pH 10-14) with saturated NaOH solution and extracted with ethyl acetate (3×200 ml). The combined organic phases were dried over Na2SO4. The solvent was removed under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399503B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-985b3c7bc27d420c8da8071c01111809 |
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| Source note | uspto-grants-2013_03 |
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