HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221975Generated: October 30, 2026
Tetrahydrofuran → HCID 59161539, compound
https://huagongshe.com/reaction/221975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl [2-(4-cyanophenyl)-5,8-dioxaspiro[3.4]oct-2-yl]carbamate | HCID 70864945 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Product | HCID 59161539 | HCID 59161539 | — |
Reaction Steps
To a solution of tert-butyl [2-(4-cyanophenyl)-5,8-dioxaspiro[3.4]oct-2-yl]carbamate (1-6) (15.0 g, 45.4 mmol) in THF (150 mL) at −78° C. was added isopropylmagnesium chloride (22.7 mL, 45.4 mmol, 2M in THF). After 1 hour, benzylmagnesium chloride (68 mL, 135 mmol, 2M in THF) was added and the reaction was allowed to slowly warm to rt over 5 hours. The reaction mixture was poured into saturated ammonium chloride, extracted with EtOAc, dried over sodium sulfate, filtered and concentrated. The crude residue was purified by column chromatography eluting with 1-60% EtOAc/Hexane. The appropriate fractions were combined and the solvent removed in vacuo to give tert-butyl {2-[4-(phenylacetyl)phenyl]-5,8-dioxaspiro[3.4]oct-2-yl}carbamate (1-7). MS (M+H)+: 424.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207169B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-ce036d4030584828bd38c133051de5d2 |
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| Source note | uspto-grants-2012_06 |
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