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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962211Generated: October 31, 2026

Diisobutylaluminum hydride → (4-Methyloxan-4-yl)methanol

https://huagongshe.com/reaction/1962211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantMethyl 4-methyloxane-4-carboxylateHCID 11019135—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product(4-Methyloxan-4-yl)methanolHCID 5970847069%

Reaction Steps

A −78° C. solution of 4-methyl-tetrahydro-pyran-4-carboxylic acid methyl ester (Regan, J. et al. J. Med. Chem. 2002, 45, 2994-3008; 9.9 g, 63 mmol) in CH2Cl2 (400 mL) was treated with DIBAL-H (1.0 M in CH2Cl2; 125 mL, 125 mmol). The resulting mixture was stirred for 1 h, and then was diluted with EtOAc (200 mL) and satd. aq. NH4Cl. The mixture was treated with satd. aq. sodium potassium tartrate, allowed to warm to rt, and stirred for 45 min. The mixture was extracted with CH2Cl2 (4×), and the combined extracts were washed with satd. aq. NaCl, dried, and concentrated. Chromatography (EtOAc/hexanes) afforded the title compound as a colorless oil (5.6 g 69%). The spectral data matched that reported in PCT Intl. Pat. Appl. Publ. No. WO 2006/001752.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415366B2
Source datasetuspto-grants-2013_04
ORD IDord-5ea00a5b2a974a538c491f84c875ef33
Source noteuspto-grants-2013_04