HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294047Generated: October 30, 2026
Tetrahydrofuran → Tert-butyl 6-triphenylmethyloxy-3(R),5(S)-dihydroxyhexanoate
https://huagongshe.com/reaction/1294047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diethylmethoxyborane | HCID 522516 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | t-Butyl (S)-5-hydroxy-3-oxo-6-(triphenylmethoxy)hexanoate | HCID 15702750 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl 6-triphenylmethyloxy-3(R),5(S)-dihydroxyhexanoate | HCID 57144739 | — |
Reaction Steps
To the crude tert-butyl 6-triphenylmethyloxy-5(S)-hydroxy-3-oxohexanoate was added 150 mL of THF followed by 15 mL of MeOH and was chilled to −60° C. 26 mL of methoxydiethylborane (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 |
|---|
| Patent number | US07238826B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-d837fa3e0b3a4cbd9584ec037cfbf126 |
|---|
| Source note | uspto-grants-2007_07 |
|---|