HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594450Generated: October 30, 2026
Acetic Acid → Tert-butyl 6-triphenylmethyloxy-3,5-dihydroxyhexanoate
https://huagongshe.com/reaction/1594450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Tert-butyl 6-triphenylmethyloxy-5-hydroxy-3-oxohexanoate | HCID 19778647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 6-triphenylmethyloxy-3,5-dihydroxyhexanoate | HCID 11374654 | — |
Reaction Steps
To the crude tert-butyl 6-triphenylmethyloxy-5-hydroxy-3-oxohexanoate was added 150 mL of THF followed by 15 mL of MeOH and was chilled to −60° C. 26 mL of MDEB (50% solution in THF) was added over a period of 20 minutes and stirring was continued for a further 30 minutes. The reaction mixture was cooled to −80° C. and 5 g of sodium borohydride was added in portions and the after completion of addition the reaction mixture was stirred for 5 hours at −78° C. Acetic acid was added to adjust the pH to 7 and water was added. The aqueous layer was extracted using EtOAC, washed with brine, dried and concentrated to give the title compound which was used as such for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07301046B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-9ab2539a0287423d8375aed3b4dd3da7 |
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| Source note | uspto-grants-2007_11 |
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